WO2012030394A1 - Treatment of myocardial infarction using tgf - beta antagonists - Google Patents

Treatment of myocardial infarction using tgf - beta antagonists Download PDF

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Publication number
WO2012030394A1
WO2012030394A1 PCT/US2011/001536 US2011001536W WO2012030394A1 WO 2012030394 A1 WO2012030394 A1 WO 2012030394A1 US 2011001536 W US2011001536 W US 2011001536W WO 2012030394 A1 WO2012030394 A1 WO 2012030394A1
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Prior art keywords
tgf
antibody
domain
seq
antagonist
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PCT/US2011/001536
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English (en)
French (fr)
Inventor
Geoffrey Y. Akita
Scott Lonning
Richard C. Gregory, Jr.
Amelia B. Kudej
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Genzyme Corporation
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Priority to CA2809568A priority Critical patent/CA2809568C/en
Priority to ES11758276T priority patent/ES2715177T3/es
Priority to KR1020137008326A priority patent/KR101939965B1/ko
Priority to NZ608813A priority patent/NZ608813A/en
Priority to AU2011296574A priority patent/AU2011296574B9/en
Priority to PL11758276T priority patent/PL2611831T3/pl
Priority to SG2013013875A priority patent/SG187953A1/en
Priority to BR112013004850A priority patent/BR112013004850B1/pt
Application filed by Genzyme Corporation filed Critical Genzyme Corporation
Priority to CN201180052346.0A priority patent/CN103201292B/zh
Priority to EP11758276.7A priority patent/EP2611831B1/en
Priority to US13/819,393 priority patent/US20130330352A1/en
Priority to RU2013114365A priority patent/RU2637088C2/ru
Priority to JP2013527063A priority patent/JP6377348B2/ja
Priority to MX2013002390A priority patent/MX354535B/es
Publication of WO2012030394A1 publication Critical patent/WO2012030394A1/en
Priority to IL225018A priority patent/IL225018A/en
Priority to US15/376,358 priority patent/US10633437B2/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/22—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against growth factors ; against growth regulators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
    • A61K39/3955—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against proteinaceous materials, e.g. enzymes, hormones, lymphokines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K48/00—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00—Drugs for disorders of the endocrine system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/545—Medicinal preparations containing antigens or antibodies characterised by the dose, timing or administration schedule
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2121/00—Preparations for use in therapy
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/475—Growth factors; Growth regulators
    • C07K14/495—Transforming growth factor [TGF]
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
    • C07K2317/21—Immunoglobulins specific features characterized by taxonomic origin from primates, e.g. man
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/76—Antagonist effect on antigen, e.g. neutralization or inhibition of binding

Definitions

  • This disclosure relates to methods of reducing adverse consequences of myocardial infarction.
  • Heart disease is the leading cause of death for both women and men in the United States. (Kung HC, Hoyert DL, Xu J, Murphy SL. Deaths: final data for 2005. National Vital Statistics Reports. 2008;56(10)). Every 34 seconds a person in the United States dies from heart disease. More than 2,500 Americans die from heart disease each day. In 2005, 652,091 people died of heart disease (50.5% of them women). This was 27.1% of all U.S. deaths. Heart disease is the leading cause of death for American Indians and Alaska Natives, blacks, Hispanics, and whites.
  • MI Myocardial infarction
  • Ischemia refers to local deficiency of blood supply, generally produced by vasoconstriction or local obstacles to blood flow. Restoration of blood flow to a previously ischemic tissue or organ, such as the heart is referred to as "reperfusion.”
  • AMI Acute myocardial infarction
  • a "heart attack” occurs when localized myocardial ischemia causes the development of a defined region of tissue death.
  • AMI is most often caused by rupture of an atherosclerotic lesion in a coronary artery. This causes the formation of a thrombus that plugs the artery, stopping it from supplying blood to the region of the heart that it supplies.
  • necrotic zone may be mainly limited to the subendocardium, typically causing non-ST segment elevation MI.
  • subendocardium about 15-30 min after onset of acute ischemia.
  • the necrotic region grows outward towards the epicardium over the next 3-6 h, eventually spanning the entire ventricular wall.
  • the myocardium may be stunned (reversibly damaged) and will eventually recover if bloodflow is restored. Contractility in the remaining viable myocardium increases, a process termed hyperkinesis.
  • the infarcted myocardium begins to undergo coagulation necrosis, a process characterized by cell swelling, organelle breakdown and protein denaturation.
  • neutrophils phagocytic lymphocytes
  • Their numbers reach a peak after about 5 days, and then decline.
  • granulation tissue appears at the edges of the infarct zone. This consists of macrophages, fibroblasts (which lay down scar tissue), and new capillaries.
  • the infarcted myocardium is especially soft between 4 and 7 days, and is therefore maximally prone to rupturing.
  • the necrotic tissue migrates inward toward the centre of the infarct over several weeks, the necrotic tissue is engulfed and digested by the macrophages. The granulation tissue then progressively matures, with an increase in connective (scar) tissue and loss of capillaries. After 2-3 months, the infarct has healed, leaving a noncontracting region of the ventricular wall that is thinned, firm and pale grey.
  • mice Microscopic morpho logic changes evolve over time as follows: Wavy myocardial fibers appear 1 - 3 hours after onset of ischemia. A staining defect with tetrazolium or basic fuchsin dye appears 2 - 3 hours after onset of ischemia. Coagulation necrosis with loss of cross stnations, contraction bands, edema, hemorrhage, and early neutrophilic infiltrate appear 4 - 12 hours after onset of ischemia. Continuing coagulation necrosis, pyknosis of nuclei, and marginal contraction bands are apparent 18 - 24 hours after onset of ischemia.
  • Total loss of nuclei and striations along with heavy neutrophilic infiltrate appears 24 - 72 hours after onset of ischemia. Macrophage and mononuclear infiltration, and, fibrovascular response begin 3 - 7 days after onset of ischemia. A fibrovascular response with prominent granulation tissue is apparent 10 - 21 days after onset of ischemia. Fibrosis is readily apparent 7 weeks or sooner after an ischemic event.
  • Complications can include: arrhythmias and conduction defects, extension of infarction or re-infarction, congestive heart failure, cardiogenic shock, pericarditis, mural thrombosis with possible embolization, myocardial wall rupture with possible tamponade, papillary muscle rupture with possible valvular insufficiency, and ventricular aneurysm formation.
  • a method of reducing an adverse consequence of myocardial infarction in a patient comprising administering an antagonist of TGF-/3 to the patient during the acute stage of the myocardial infarction.
  • the myocardial infarction is an acute myocardial infarction.
  • Administration of the antagonist of TGF-/3 may be commenced within 120 hours of onset of acute myocardial ischemia. In various embodiments, administration of the antagonist of TGF-/3 is commenced within about 72 hours, within about 48 hours, within about 24 hours, or within about 12 hours of onset of acute myocardial ischemia.
  • Administration of the antagonist of TGF-/3 may be commenced prior to substantial macrophage and mononuclear infiltration of tissue affected by the myocardial infarction. In some embodiments, administration of the antagonist of TGF-/3 is commenced during a period characterized by neutrophilic infiltration of tissue affected by the myocardial infarction. In other embodiments, administration of the antagonist of TGF- 3 is commenced during a period characterized by necrosis of tissue affected by the myocardial infarction. Generally, the patient may be a human or a non-human mammal.
  • the TGF-/3 antagonist may be selected from the group consisting of: (i) an antibody or antibody fragment that specifically binds to one or more isoforms of TGF-/3; (ii) a TGF-/3 receptor or soluble fragment thereof; (iii) an antibody or antibody fragment that specifically binds to one or more TGF-/3 receptors; and (iv) an antisense or interfering RNA oligonucleotide.
  • the method further comprises administering a compound that is capable of selectively restoring a desirable function of TGF- 3 to the patient.
  • a compound capable of selectively restoring a desirable function of TGF-/3 may be an anti-inflammatory drug, or an antagonist of TNF- ⁇ x
  • the method may include administering an ACE inhibitor to the patient.
  • the ACE inhibitor may be selected from the group consisting of benazepril, captopril, fosinopnl, moexipril, penndopril, quinapril, transdolapril, lisinopril, enalapril and ramparil.
  • the method may further comprise administering an angiotensin ⁇ receptor antagonist to the patient.
  • the angiotensin ⁇ receptor antagonist may be selected from the group consisting of eprosartan, telmisartan, losartan, irbesartan, olmesartan, candesartan, and valsartan.
  • the TGF-jS antagonist may be an antibody or antibody fragment that specifically binds to one or more isoforms of TGF-/3 and may neutralize one or more of human TGF-/31, TGF- 32 and TGF-/33.
  • the antibody or antibody fragment may comprise a PET1073G12 VH domain (SEQ ID NO: 2) with up to 5 mutations, or an antigen-binding portion thereof.
  • the antibody or antibody fragment comprises a PET1074B9 VH domain (SEQ ID NO: 12) with up to 5 mutations, or an antigen-binding portion thereof.
  • the antibody or antibody fragment comprises a PET1287A10 VH domain (SEQ ID NO: 22) with up to 5 mutations, or an antigen-binding portion thereof.
  • the antibody or antibody fragment comprises the PET1073G12 VL domain (SEQ ID NO: 7) with up to 5 mutations, or an antigen-binding portion thereof.
  • the antibody or antibody fragment comprises the PET1074B9 VL domain (SEQ ID NO: 17) with up to 5 mutations, or an antigen-binding portion thereof.
  • the antibody or antibody fragment comprises the PET1287A10 VL domain (SEQ ID NO: 27) with up to 5 mutations, or an antigen-binding portion thereof.
  • the antibody or antibody fragment comprises the PET 1073G12 VH domain (SEQ ID NO: 2) and the PET 1073G12 VL domain (SEQ ID NO: 7). In some embodiments, the antibody or antibody fragment comprises the PET 1074B9 VH domain (SEQ ID NO: 12) and the PET 1074B9 VL domain (SEQ ID NO: 17). In some embodiments, the antibody or antibody fragment comprises the PET 1287A10 VH domain (SEQ ID NO: 22) and the PET 1287A10 VL domain (SEQ ID NO: 27).
  • the antibody or antibody fragment comprises a set of CDRs (HCDRl, HCDR2 and HCDR3), wherein said HCDR3 has an amino acid sequence selected from the group consisting of SEQ ID NO: 5, SEQ ID NO: 15 and SEQ ID NO: 25.
  • the HCDRl, HCDR2 and HCDR3 of the VH domain are within a germline heavy chain framework.
  • the HCDRl, HCDR2 and HCDR3 of the VH domain are within a framework that comprises up to 12 mutations from the germline amino acid sequence.
  • the antibody or antibody fragment comprises a set of CDRs (LCDRl, LCDR2 and LCDR3), wherein said LCDR3 has an amino acid sequence selected from the group consisting of SEQ ID NO: 10, SEQ ID NO: 20 and SEQ ID NO: 30.
  • the LCDRl, LCDR2 and LCDR3 are within a germline heavy chain framework.
  • the LCDRl, LCDR2 and LCDR3 are within a framework that comprises up to 5 mutations from the germline amino acid sequence.
  • FIG. 1 shows a reduction in fibrosis with administration of 1D11-D3 and
  • FIG. 2 shows anterior wall thickening and posterior wall thickening in an echocardiogram analysis.
  • FIG. 3 shows a regional wall motion score in an echocardiogram analysis.
  • FIG. 4 shows a reduction in fibrosis with administration of ID 1 1 and 13C4.
  • FIG. 5 shows anterior wall thickening and posterior wall thickening in an echocardiogram analysis for 13C4-D0, 1D11-D0, 13C4-D1, 1D11-D1, 13C4-D5 and 1D11- D5 treated groups.
  • FIG. 6 shows a regional wall motion score in an echocardiogram analysis for vehicle, 13C4 - D0, 1D11 - DO, 13C4 - D1, 1D11 - Dl, 13C4 - D5 and 1D11 - D5 treated groups.
  • FIG. 7 shows LV scar volume as compared to vehicle-treated groups.
  • FIG 8 shows the number of TU EL positive cells in the area adjacent to the scar.
  • FIG. 9 shows the LV ejection fraction (LVEF), measured at 4 weeks after coronary artery occlusion/coronary artery reperfusion (CAO/CAR).
  • FIG 10 shows the LVEF measured at 2-4 weeks after CAO/CAR.
  • FIG. 11 shows LV isovolumetric relaxation time.
  • FIG. 12 shows regional wall thickening as compared to vehicle.
  • FIG. 13 shows the slopes of LV-end-diastolic pressure-volume relationship.
  • FIG. 14 shows a reduction in fibrosis in the LV with administration of 1D1 1 at doses of 1 and 5 mg/kg from two different formulations.
  • FIG. 15 shows a reduction in fibrosis with in the area at risk with administration of ID 11 at doses of 1 and 5 mg/kg from two different formulations.
  • FIG. 16 shows an increase of myocardium in the area at risk
  • FIG. 17 shows the regional wall motion score in an echocardiogram analysis for vehicle, 13C4 and 1D1 1 at 1 and 5 mg/kg for both formulations.
  • FIG. 18 shows dose-dependent serum levels of 1D11 following IV
  • FIG. 19 shows reductions in serum osteopontin with administration of ID 11 post I/R.
  • FIG. 20 shows induction of TGF- ⁇ following IR and dose-dependent 1D11- mediated reduction of TGF- ⁇ following I/R.
  • FIG. 21 shows induction of TGF-P2 following IR and dose-dependent 1D11- mediated reduction of TGF- 21 following I/R.
  • FIG 22 shows induction of TGF-p3 following IR and dose-dependent 1D1 1- mediated reduction of TGF-b3 following I/R.
  • FIG 23 shows induction of collagen 3 following IR and dose-dependent 1D11- mediated reduction of collagen 3 following I/R.
  • FIG 24 shows induction of endothelin-1 following IR and dose-dependent
  • FIG 25 shows induction of plasminogen activator inhibitor- 1 following IR and dose-dependent ID 11 -mediated reduction of plaminogen activator inhibitor- 1 following I R.
  • FIG 26 shows induction of Snaill following JR. and dose-dependent 1D1 1- mediated reduction of Snaill following I/R.
  • FIG 27 shows induction of Snail2 following DR. and dose-dependent 1D1 1- mediated reduction of Snail2 following I/R.
  • FIG 28 shows induction of a-smooth muscle actin following JR and dose- dependent ID 11 -mediated reduction of a-smooth muscle actin following I/R.
  • FIG 29 shows induction of fibronectin following JR and dose-dependent
  • FiG 30 shows effect of administration of 5 mg/kg 1D1 1 on the expression of
  • the heart After a MI, or heart attack, the heart starts to repair itself.
  • This cardiac repair process can be separated into overlapping phases.
  • the first phase is known as the
  • the inflammatory phase Following the inflammatory phase is the proliferative phase.
  • the maturation phase is the last phase of heart repair.
  • the inflammatory phase is characterized by cardiomyocyte death, induction of cytokines and chemokines, and an influx of
  • the proliferative phase there is suppression of inflammatory mediators as well as an influx of cells that contribute to the formation of connective tissue fibers, fibroblasts, and endothelial cells into the infarcted area. Fibroblasts secrete extracellular matrix. The endothelial cells contribute to the formation of a microvascular network within the developing loose fibrous connective tissue, or granulation tissue. Infiltrated inflammatory cells then begin to undergo cell death, or what is known as apoptosis. Finally, during the maturation phase the granulation tissue from the proliferative phase organizes and matures into a dense fibrous connective tissue scar. This remodeling of the fibrotic response in the myocardium can be prolonged. In general, the inflammatory phase occurs from the time of infarction to 1-7 days post-MI. The proliferative phase occurs from approximately 5-14 days post-MI. Finally, the maturation phase starts from
  • TGF- ⁇ is induced in infarcted myocardium and participates in all phases of post-MI repair, which has complicated attempts to define the role of this cytokine in cardiac repair.
  • TGF-/3 is a multifunctional cytokine originally named for its ability to transform normal fibroblasts to cells capable of anchorage-independent growth.
  • TGF-/31 is a multifunctional cytokine originally named for its ability to transform normal fibroblasts to cells capable of anchorage-independent growth.
  • TGF-/31 TGF- 32, TGF- 33, TGF-/34, and TGF- 35.
  • TGF-/5s from various species including humans, mice, green monkeys, pigs, cows, chicks, and frogs. It is also possible to purify this family of TGF-/3s from various body sources including bone, platelets, or placenta, for producing it in recombinant cell culture, and for determining its activity.
  • TGF-/31 In humans, three isoforms, TGF-/31, TGF-/32 and TGF-03, are known to exist.
  • TGF-/31 differs from TGF- ⁇ 2 by 27 amino acids, and from TGF-/33 by 22 amino acids. The differences are mainly conservative amino acid changes.
  • the three-dimensional structure of TGF-/3 has been determined by X-ray crystallography and the receptor binding regions have been defined. Both human TGF-/3s and mouse TGF-/3s are similar.
  • the human TGF-/31 has one amino acid difference from a mouse TGF-/31.
  • Human TGF-/32 has only a three amino acid difference from mouse TGF-/32, and human and mice TGF-/33 are identical.
  • TGF-/3 or "transforming growth factor-beta” refers to the family of molecules described that have either the full-length, native amino acid sequence of any of the humans TGF-/3 isoforms. These include the latent forms (“latent TGF-/3 ”) and associated or unassociated complex of precursors and mature TGF-/3.
  • TGF-/3 will be understood to be a reference to any one of the currently identified forms, including TGF-/31, TGF-/32, TGF-/33, TGF-/34, and TGF-/35 and latent versions thereof, as well as to human TGF-/3 species identified in the future, including polypeptides derived from the sequence of any known TGF-/3 and being at least about 75%, preferably at least about 80%, more preferably at least about 85%, still more preferably at least about 90%, and even more preferably at least about 95% homologous with the sequence.
  • TGF-/31 refers to the TGF-/& defined in the literature (e.g., Derynck et al., Nature, supra, Seyedin et al., J. Biol. Chem., 262, supra, and deMartin et al., supra).
  • TGF-/3 refers to the gene encoding human TGF-/3.
  • TGF- ⁇ family are proteins that have nine cysteine residues in the mature portion of the molecule, share at least 65% homology with other known TGF-/3 sequences in the mature region, and may compete for the same receptor. In addition, they all appear to be encoded as a larger precursor that shares a region of high homology near the N- terminus and shows conservation of three cysteine residues in the portion of the precursor that will later be removed by processing. TGF-/3 family members also appear to have a processing site with four or five amino acids.
  • An increase in the level of TGF-/3 activity is involved in a large number of pathologic conditions, including, but not limited to, the following: (i) fibrosis, scarring, and adhesion during wound healing; (ii) fibrotic diseases of the heart, lungs, liver, and kidneys; (iii) atherosclerosis and arteriosclerosis; (iv) certain types of cancer including cancer of the prostate, neuroendocrine tumors of the digestive system, cancer of the cervix, glioblastomas, and gastric cancer; (v) angiopathy, vasculopathy, nephropathy; (vi) systemic sclerosis; (vii) viral infection, such as hepatitis C and HIV; and (viii) immunological and inflammatory disorders and deficiencies, such as rheumatoid arthritis.
  • pathologic conditions including, but not limited to, the following: (i) fibrosis, scarring, and adhesion during wound healing; (ii) fibrotic diseases of the heart, lungs, liver
  • TGF-/3 was administered in models of myocardial ischemic injury within a few hours after ischemic injury.
  • Lefer showed in isolated rat hearts that administration of TGF-/3 before, or immediately after ischemic cardiac injury reduced superoxide anions in coronary circulation, maintained endothelial-dependent coronary relaxation, reduced injury mediated from exogenous tumor necrosis factor (TNF), and prevented severe cardiac injury.
  • TNF tumor necrosis factor
  • TGF-/3 preserved endothelial function, particularly by maintenance of endothelium-derived relaxation factor (EDRF but now known as nitric oxide or NO) formation by the endothelium.
  • EDRF endothelium-derived relaxation factor
  • TGF- ⁇ receptor antagonists to interrupt TGF-/3 signaling.
  • Ikeuchi et al. (Cardiovascular Research, 64:526-35, 2004) blocked TGF-0 signaling at the time of MI by intramuscular injection of a plasmid encoding the extracellular domain of the TGF- 3 type II receptor (T/3IJR) in mice 7 days prior to MI. They observed increased mortality during the 24 hours after MI, increased inflammation, increased left ventricle (LV) dilation and contractile dysfunction despite no increase in infarct size as compared to untreated mice.
  • T/3IJR TGF- 3 type II receptor
  • mice received intramuscular injections of T/3HR at either day 0 or day 7 after MI.
  • T/3IIR treatment prevented LV dilatation, contractile dysfunction, cardiomyocyte hypertrophy and interstitial fibrosis in the noninfarcted myocardium.
  • TGF-/3 was beneficial in early phase but the benefits were lost with sustained expression, leading to LV remodeling and failure.
  • mice intramuscularly with an adenovirus encoding a soluble TGF- 3 type ⁇ receptor
  • TGF- ⁇ antagonism using an antagonist antibody effective against TGF- ⁇ , 2 and 3 was investigated in MI repair.
  • Frantz et al (Basic Research in Cardiology, 103:485-502, 2008) administered the TGF- ⁇ antagonist antibody or a negative-control antibody to mice starting at either 7 days prior to, or 5 days after, induction of MI by coronary artery ligation.
  • the antibodies were administered every other day throughout the 8 week duration of the study. Mortality was significantly higher in the groups that received the anti-TGF- ⁇ antibody.
  • both anti-TGF- ⁇ antibody treated groups demonstrated increased left ventricular dilatation.
  • a method of treating a patient suffering from myocardial infarction, particularly acute myocardial infarction, or of reducing an adverse consequence of myocardial infarction in a patient comprising administering an antagonist of TGF-/3 to the patient during the acute stage of the myocardial infarction.
  • administration of the antagonist of TGF-/3 may be advantageously commenced at a time less than 120 hours after the onset of acute myocardial ischemia is surprising.
  • the methods described herein contemplate that administration of the antagonist of TGF-/3 may be commenced within about 72 hours, within about 48 hours, within about 24 hours, or within about 12 hours of onset of acute myocardial ischemia.
  • a TGF- ⁇ antagonist is administered during the acute phase of MI.
  • Administration of the antagonist of TGF-/3 may be commenced prior to substantial macrophage and mononuclear infiltration of tissue affected by the myocardial infarction. In some embodiments, administration of the antagonist of TGF-/3 is commenced during a period characterized by neutrophilic infiltration of tissue affected by the myocardial infarction. In other embodiments, administration of the antagonist of TGF-/3 is commenced during a period characterized by necrosis of tissue affected by the myocardial infarction.
  • Treatment refers to both therapeutic treatment and prophylactic or preventative measures. Those in need of treatment include those already with a treatable disorder as well as those in which the disorder is to be prevented. Treatment may or may not comprise a complete cure or recovery of normal function. Treatment may also comprise amelioration of undesired symptoms and/or a reduction in adverse consequences of a disorder.
  • a "mammal” can be any animal classified as a mammal, including humans, domestic and farm animals, and zoo, sports, or pet animals, such as dogs, horses, cats, cows, etc. Preferably, the mammal is a primate, such as a monkey, ape, or human, for example.
  • the term "effective amount” refers to an amount of a drug effective to treat a disease or disorder in a mammal.
  • TGF-/3 functions may be desired in the early phase post-MI, antagonism of TGF during the acute period and beyond can result in improved cardiac remodeling and function.
  • a TGF- ⁇ antagonist another compound that is capable of selectively restoring a desirable function of TGF-/3.
  • a compound capable of selectively restoring a desirable function of TGF-/3 may be an anti-inflammatory drug, or an antagonist of TNF- ⁇ . It may also be desirable to coadminister another treatment, for example, the method may include administering an ACE inhibitor to the patient.
  • the ACE inhibitor may be selected from the group consisting of benazepril, captopril, fosinopril, moexipril, perindopril, quinapril, transdolapril, lisinopril, enalapril and ramparil.
  • the method may further comprise
  • angiotensin ⁇ receptor antagonist may be selected from the group consisting of eprosartan, telmisartan, losartan, irbesartan, olmesartan, candesartan, and valsartan.
  • Neutralizing antibodies can be used as TGF- ⁇ antagonists.
  • An "antibody” is an immunoglobulin whether natural or partly or wholly synthetically produced. The term also covers any polypeptide or protein comprising an antigen-binding domain of an antibody.
  • Antibody fragments which comprise an antigen-binding domain are molecules, such as Fab, scFv, Fv, dAb, Fd and diabodies.
  • antibody is used in the broadest sense and specifically covers intact monoclonal antibodies, polyclonal antibodies, multispecific antibodies (e.g., bispecific antibodies) formed from at least two intact antibodies, and antibody fragments, so long as they exhibit the desired biological activity.
  • Monoclonal antibodies are highly specific, being directed against a single antigenic site.
  • polyclonal antibody preparations that include different antibodies directed against different determinants (epitopes)
  • each monoclonal antibody is directed against a single determinant on the antigen.
  • monoclonal antibodies are advantageous in that they may be synthesized uncontaminated by other antibodies.
  • the modifier "monoclonal” indicates the character of the antibody as being obtained from a substantially homogeneous population of antibodies, and is not to be construed as requiring production of the antibody by any particular method.
  • monoclonal antibodies may be made by the hybridoma method first described by Kohler et al., Nature, 256:495 (1975), or may be made by recombinant DNA methods (see, e.g., U.S. Pat. No. 4,816,567).
  • the “monoclonal antibodies” may also be isolated from phage antibody libraries using the techniques described in Clackson et al., Nature, 352: 624-628 (1991) and Marks et al., J. Mol.
  • Antibody fragments comprise a portion of an intact antibody, preferably comprising the antigen-binding or variable region thereof.
  • antibody fragments include Fab, Fab', F(ab')2, and Fv fragments; diabodies; linear antibodies; single-chain antibody molecules; and multispecific antibodies formed from antibody fragment(s).
  • Fc receptor or "FcR” are used to describe a receptor that binds to the Fc region of an antibody.
  • the preferred FcR is a native-sequence human FcR.
  • variable in the context of an antibody or antibody fragment refers to the fact that certain portions of the variable domains differ extensively in sequence among antibodies and are used in the binding and specificity of each particular antibody for its particular antigen. However, the variability is not evenly distributed throughout the variable domains of antibodies. It is concentrated in three segments called hypervariable regions both in the light-chain and the heavy-chain variable domains. The more highly conserved portions of variable domains are called the framework regions (FRs).
  • the variable domains of native heavy and light chains each comprise four FRs, largely adopting a /3-sheet configuration, connected by three hypervariable regions, which form loops connecting, and in some cases forming part of, the /3-sheet structure.
  • hypervariable region refers to the amino acid residues of an antibody that are responsible for antigen-binding.
  • the hypervariable region generally comprises amino acid residues from a “complementarity-determining region” or "CDR.”
  • “Framework Region” or "FR” residues are those variable-domain residues other than the hypervariable region residues as herein defined.
  • Fv is the minimum antibody fragment that contains a complete antigen- recognition and antigen-binding site. This region consists of a dimer of one heavy-chain and one light-chain variable domain in tight, non-covalent association. It is in this configuration that the three hypervariable regions of each variable domain interact to define an antigen- binding site on the surface of the VH-VL dimer. Collectively, the six hypervariable regions confer antigen-binding specificity to the antibody. However, even a single variable domain (or half of an Fv comprising only three hypervariable regions specific for an antigen) has the ability to recognize and bind antigen, although at a lower affinity than the entire binding site.
  • the Fab fragment also contains the constant domain of the light chain and the first constant domain (CHI) of the heavy chain.
  • Fab' fragments differ from Fab fragments by the addition of a few residues at the carboxy terminus of the heavy-chain CHI domain including one or more cysteines from the antibody hinge region.
  • Fab'-SH is the designation herein for Fab' in which the cysteine residue(s) of the constant domains bear at least one free thiol group.
  • F(ab')2 antibody fragments originally were produced as pairs of Fab' fragments that have hinge cysteines between them. Other chemical couplings of antibody fragments are also known.
  • the "light chains” of antibodies from any vertebrate species can be assigned to one of two clearly distinct types, called kappa ( ⁇ ) and lambda ( ⁇ ), based on the amino acid sequences of their constant domains.
  • "Single-chain Fv” or “scFv” antibody fragments comprise the VH and VL domains of antibody, wherein these domains are present in a single polypeptide chain.
  • humanized forms of non-human (e.g., rodent) antibodies are chimeric antibodies that contain minimal sequence derived from non-human immunoglobulin.
  • humanized antibodies are human immunoglobulins (recipient antibody) in which residues from a hypervariable region of the recipient are replaced by residues from a hypervariable region of a non-human species (donor antibody), such as mouse, rat, rabbit, or non-human primate having the desired specificity, affinity, and capacity.
  • donor antibody such as mouse, rat, rabbit, or non-human primate having the desired specificity, affinity, and capacity.
  • framework region (FR) residues of the human immunoglobulin are replaced by corresponding non-human residues.
  • humanized antibodies may comprise residues that are not found in the recipient antibody or in the donor antibody. These modifications are made to further refine antibody performance.
  • the humanized antibody will comprise substantially all of at least one, and typically two, variable domains, in which all or substantially all of the hypervariable loops correspond to those of a non-human
  • immunoglobulin and all or substantially all of the FRs are those of a human immunoglobulin sequence.
  • the humanized antibody optionally also will comprise at least a portion of an immunoglobulin constant region (Fc), typically that of a human immunoglobulin.
  • Fc immunoglobulin constant region
  • TGF-/3 antibody refers to an antibody that binds to any of the isoforms of
  • TGF-/3 preferably binding to either TGF-/31, TGF-/32, or TGF-/33, or to any combination thereof, more preferably at least TGF-/31, or at least TGF-/32, and most preferably TGF- 31, or TGF- 31 together with TGF-/32.
  • the antibody may bind to at least TGF- 33.
  • TGF-/33 isoforms is known as 1D11 and is available from R&D Systems- (Catalog No. MAB- 1835) of through the ATCC (Accession No. HB 9849).
  • a mouse monoclonal antibody directed against human TGF-/31 is also available from R&D Systems.
  • Neutralizing mouse monoclonal antibodies have also been generated from mice immunized with human TGF-/31 peptides comprising amino acid positions 48 to 60 (antibody reactive with TGF-/31, TGF-/32 and TGF-/33) and amino acid positions 86 to 101 (antibody specific for TGF- 31). (Hoefer and Heat, Cancer Immunol. Immunother., 41 : 302-308 (1995)).
  • GC1008 is a humanized monoclonal IgG4 antibody that neutralizes all TGF-/3 isoforms and is suitable for therapeutic use in humans.
  • 1D11 is a murine pan- specific anti-TGF-/3 antibody that neutralizes mouse
  • TGF-/31, TGF-/32 and TGF-/33 and human TGF-/31 and TGF-/32 in a wide range of in vitro assays U.S. Patent No. 5,571,714; R&D System product sheet for MAB1835).
  • 1D11 In animal models of fibrosis, 1D11 has proven efficacious. However, 1D11 is a murine monoclonal antibody and may be unsuitable for therapeutic use in humans. Thus, in some embodiments a human antibody or a modified antibody comprising human sequence elements may be desired.
  • methods of treating MI can comprise administration of antibodies against TGF- ⁇ to treat acute fibrosis that is associated with overproduction of TGF-/3 in TGF- ⁇ related diseases.
  • the body responds to injury or disease by regenerating destroyed tissues. When the injury is prolonged or extensive, the destroyed tissue may be replaced by specialized fibrotic connective tissue. The deposition of this fibrotic tissue may result in an impairment of the affected tissue or organ function in the patient.
  • Administration of an effective amount of anti-TGF- ⁇ antibody during the acute phase can reduce the subsequent development of fibrosis.
  • an effective amount of anti-TGF- ⁇ antibody may also be administered during the period of post-MI recovery that is typically characterized by fibrosis to neutralize the biologic activity of TGF-/3, thereby reducing fibrotic development.
  • the TGF-/3 antagonist may be selected from the group consisting of: (i) an antibody or antibody fragment that specifically binds to one or more isoforms of TGF- ⁇ ; (ii) a TGF-/3 receptor or soluble fragment thereof; (iii) an antibody or antibody fragment that specifically binds to one or more TGF-/3 receptors; and (iv) an antisense or interfering RNA oligonucleotide.
  • Anti-TGF- ⁇ antibodies that specifically bind and neutralize a TGF-/3 molecule are particularly useful as TGF- 3 antagonists. Examples of such antibodies are described in U.S. Patent Application Publication No. 2006/0251658.
  • Anti-TGF- ⁇ antibodies include specific antibodies for TGF- ⁇ , in particular human TGF- ⁇ including specific antibodies that are directed to TGF- ⁇ , TGF ⁇ 2 and TGF ⁇ 3.
  • antibody molecule should be construed as covering any antibody or substance having an antigen- binding site of an antibody with the required specificity.
  • this term covers antibody fragments and derivatives, including any polypeptide comprising an antigen-binding domain, whether natural or wholly or partially synthetic. Chimeric molecules comprising an antigen- binding domain of an antibody, or equivalent, fused to another polypeptide are therefore included. Cloning and expression of chimeric antibodies are described in EP-A-0120694 and EP-A-0125023, and a large body of subsequent literature.
  • anti-TGF-jS antibody is broadly used herein to include whole antibodies (e.g., IgG, such as IgGl or IgG4), antibody fragments (e.g., scFv, Fab, dAb), or molecules comprising an anti-TGF-0 antigen-binding site derived from an anti-TGF-/3 antibody or components thereof.
  • whole antibodies e.g., IgG, such as IgGl or IgG4
  • antibody fragments e.g., scFv, Fab, dAb
  • molecules comprising an anti-TGF-0 antigen-binding site derived from an anti-TGF-/3 antibody or components thereof.
  • Antagonists of TGF- ⁇ include humanized monoclonal anti-TGF- ⁇ antibodies having one or more amino acid residues and introducing into it from a source that is non- human. Humanization can be performed following the method of Winter and co-workers (Jones et al, Nature, 321 : 522-525 (1986); Riechmann et al., Nature, 332: 323-327 (1988); Verhoeyen et al., Science, 239: 1534-1536 (1988)), by substituting hypervariable region sequences for the corresponding sequences of a human antibody. Accordingly, such
  • humanized antibodies may be chimeric antibodies (for example, as described in U.S. Pat. No. 4,816,567) wherein substantially less than an intact human variable domain has been substituted by the corresponding sequence from a non-human species.
  • humanized antibodies are typically human antibodies in which some hypervariable region residues and possibly some FR residues are substituted by residues from analogous sites in rodent antibodies.
  • the sequence of the variable domain of a rodent antibody is screened against the entire library of known human variable- domain sequences.
  • the human sequence that is closest to that of the rodent is then accepted as the human framework region (FR) for the humanized antibody (Sims et al., J. Immunol., 151 : 2296 (1993); Chothia et al, J. Mol. Biol., 196: 901 (1987)).
  • Another method uses a particular framework region derived from the consensus sequence of all human antibodies of a particular subgroup of light or heavy chains. The same framework may be used for several different humanized antibodies (Carter et al., Proc. Natl. Acad. Sci. USA, 89:4285 (1992); Presta et al., J. Immunol., 151 : 2623 (1993)).
  • humanized antibodies retain high affinity for the antigen and other favorable biological properties.
  • humanized antibodies can be prepared by a process comprising analysis of the parental sequences and various conceptual humanized products using three-dimensional models of the parental and humanized sequences. Three- dimensional immunoglobulin models are commonly available and are familiar to those skilled in the art. Computer programs are available that illustrate and display probable three- dimensional conformational structures of selected candidate immunoglobulin sequences. Inspection of these displays permits analysis of the likely role of the residues in the
  • FR residues can be selected and combined from the recipient and import sequences so that the desired antibody characteristic, such as increased affinity for the target antigen(s), is achieved.
  • the hypervariable region residues are directly and most substantially involved in influencing antigen binding.
  • Anti-TGF- ⁇ antibodies typically comprise antibody VH and VL domains.
  • VH and VL domains are complementarity determining regions, CDRs, which may be comprised within different framework regions, FR's, to form VH or VL domains as the case may be.
  • An antigen-binding site may consist of an antibody VH domain and/or a VL domain or antigen-binding portions thereof.
  • An anti-TGF- ⁇ antibody can comprise an HCDR set, an LCDR set, or both and/or a human antibody VH domain, VL domain or both.
  • a set of HCDR1 , HCDR2 and HCDR3 may have sequences selected from the following sets:
  • HCDR1 SEQ ID NO: 3 HCDR2 SEQ ID NO: 4
  • HCDR3 SEQ ID NO: 5 (referred to herein as the "PET1073G12 set of HCDRs");
  • HCDR1 SEQ ID NO: 13, HCDR2 SEQ ID NO: 14, HCDR3 SEQ ID NO: 15 (referred to herein as the "PET1074B9 set of HCDRs");
  • HCDR1 SEQ ID NO: 23 HCDR2 SEQ ID NO: 24, HCDR3 SEQ ID NO: 25 (referred to herein as the "PET1287A10 set of HCDRs").
  • a set of LCDRl , LCDR2 and LCDR3 may have sequences selected from the following sets:
  • LCDRl SEQ ID NO: 8 LCDR2 SEQ ID NO: 9, LCDR3 SEQ ID NO: 10 (referred to herein as the "PET1073G12 set of LCDRs");
  • LCDRl SEQ ID NO: 18, LCDR2 SEQ ID NO: 19, LCDR3 SEQ ID NO: 20 (referred to herein as the "PET1074B9 set of LCDRs");
  • LCDRl SEQ ID NO: 28 LCDR2 SEQ ID NO: 29, LCDR3 SEQ ID NO: 30 (referred to herein as the "PET1287A10 set of LCDRs").
  • a VH domain comprising a set of HCDRs as disclosed herein may comprise separately a VL domain comprising a set of LCDRs as disclosed herein.
  • VH domain is paired with such a VL domain, and most preferably the VH and VL domain pairings are the same as in the clones as set out herein.
  • a VH domain of an anti-TGF- ⁇ antibody can contain a set of HCDRs
  • HCDR1, HCDR2 and HCDR3 wherein the set of HCDRs corresponds to that for
  • PET1073G12, PET1074B9 or PET1287A10 with one or two amino acid substitutions are provided.
  • An anti-TGF- ⁇ antibody can comprise a VL domain comprising a set of
  • LCDRs LCDR1, LCDR2 and LCDR3 wherein the set of CDRs corresponds to that for PET1073G12, PET1074B9 or PET1287A10 with one or two amino acid substitutions.
  • the properties of antibodies can be derived from empirical and theoretical models of antibody sequence, functional and three-dimensional structures (for example, analysis of likely contact residues or calculated physicochemical property) and these properties can be considered singly and in combination.
  • sequence-structure relationship can be used for prediction of those residues in an antibody of known sequence, but of an unknown three-dimensional structure, which are important in maintaining the three-dimensional structure of its CDR loops and hence in maintaining binding specificity. These predictions can be confirmed by comparison of the predictions to the output from lead optimization experiments.
  • a theoretical model can be created of the antibody molecule (Chothia, et al. Science, 223,755- 758 (1986)) using any freely available or commercial package, such as WAM (Whitelegg, N.R.u. and Rees, A. R (2000) Prot. Eng., 12, 815-824).
  • a protein visualisation and analysis software package such as Insight ⁇ (Accelerys, Inc.) or Deep View (Guex, N. and Peitsch, M. C. Electrophoresis (1997) 18, 2714-2723) may then be used to evaluate possible substitutions at each position in the CDR and FR. This information may then be used to make
  • substitutions likely to have a minimal or beneficial effect on activity.
  • the techniques required to make substitutions within amino acid sequences of CDRs, antibody VH or VL domains and specific antibodies generally is available in the art.
  • Variant sequences may be made, with substitutions that may or may not be predicted to have a minimal or beneficial effect on activity.
  • an anti-TGF- ⁇ antibody can comprise a defined set of CDRs, in particular the set of CDRs of PET1073G12, PET1074B9 and PET1287A10, and sets of CDRs of PET1073G12, PET1074B9 or PET1287A10 with one or two substitutions within the set of CDRs.
  • the relevant set of CDRs is provided within antibody framework regions or other protein scaffolds, e.g., fibronectin or cytochrome B. Preferably antibody framework regions are employed.
  • the heavy chain of an anti-TGF- ⁇ antibody can utilize a human VH I family gene.
  • the heavy chain framework amino acid sequence contains 1- 12, preferably 3-12 and more preferably 3-8 amino acid differences as compared to the germline amino acid sequence of the human VH I family gene.
  • the heavy chain framework sequence is the germline sequence.
  • the antibody framework region for the heavy chain may be human DP- 10 (VH 1-69) or human DP-88 (VH 1 -e) from the V H 1 family.
  • Some embodiments utilizing a human DP- 10 gene have a non-germline amino acid at residues 27, 78 and 94.
  • residue 27 is tyrosine
  • residue 78 is threonine
  • residue 94 is serine or leucine.
  • the light chain utilizes a human VK3 family gene with 1-5, 1- 4, more preferably 1-3 amino acid differences as compared to the germline amino acid sequence.
  • the light chain framework sequence is the germline human V K 3 family gene sequence.
  • the framework region for the light chain may be human DPK-22 (A27).
  • residue 2 is a non- germline amino acid.
  • residue 2 is a threonine.
  • a VH domain is provided with the amino acid sequence of SEQ ID NO: 2, this being termed “PET1073G12 VH domain,” or SEQ ID NO: 12, this being termed “PET1074B9 VH domain,” or SEQ ID NO: 22, this being termed “PET1287A10 VH domain.”
  • a VL domain comprises the amino acid sequence of
  • antibody TGF-j8-binding site may be comprised within any desired antibody molecule format, e.g., scFv, Fab, IgGl, IgG4, dAb etc., as is discussed further elsewhere herein.
  • an IgG4 antibody molecule comprising the PET1073G12, PET1074B9 or PET1287A10 VH domain, preferably also comprising the corresponding PET1073G12, PET1074B9 or PET1287A10 VL domain.
  • PET1074B9 or PET1287A10 VH domain and/or the PET1073G12, PET1074B9 or
  • PET1287A10 VL domain are further examples as are other antibody molecules comprising the PET1073G12, PET1074B9 or PET1287A10 set of HCDRs within an antibody VH domain, and/or the PET1073G12, PET1074B9 or PET1287A10 set of LCDRs within an antibody VL domain.
  • An anti-TGF-jS antibody may be an antibody which binds all three isoforms of human TGF- ⁇ .
  • Such an anti-TGF-/3 antibody can comprise the PET1073G12, PET1074B9 or PET1287A10 VH and/or VL domain or antigen-binding portions of those domains.
  • a VH domain from one of the above is paired with a VL domain from one of the above to provide an antigen-binding site.
  • the PET1073G12 VH domain SEQ ID NO: 2
  • the PET1073G12 VL domain SEQ ID NO: 7
  • the PET1074B9 VH domain (SEQ ID NO: 12) is paired with the PET1074B9 VL domain (SEQ ID NO: 17), so that an antigen-binding site is formed comprising both the PET1074B9 VH and VL domains.
  • the PET1287A10 VH domain (SEQ ED NO: 22) is paired with the PET1287A10 VL domain (SEQ ED NO: 27), so that an antigen-binding site is formed comprising both the PET1287A10 VH and VL domains.
  • a PET1073G12, PET1074B9 or PET1287A10 VH domain is paired with a VL domain other than the corresponding PET1073G12,
  • PET1074B9 or PET1287A10 VL are PET1074B9 or PET1287A10 VL.
  • any set of HCDRs disclosed herein can be provided in a VH domain that is used as a specific antibody alone or in combination with a VL domain.
  • a VH domain may be provided with a set of HCDRs as disclosed herein, and if such a VH domain is paired with a VL domain, then the VL domain may be provided with a set of LCDRs disclosed herein.
  • a pairing of a set of HCDRs and a set of LCDRs may be as disclosed herein for the PET1073G12, PET1074B9 and PET1287A10 antibodies.
  • the framework regions of the VH and/or VL domains may be germline frameworks.
  • Frameworks regions of the heavy chain domain may be selected from the VH-1 family, and a preferred V H - I framework is DP- 10 or DP-88 framework.
  • Framework regions of the light chain may be selected from the VK3 family, and a preferred such framework is DPK-22.
  • One or more CDRs may be taken from a VH or VL domain of which the sequence is disclosed herein and incorporated into a suitable framework. This is discussed further herein. The same applies for other CDRs and sets of CDRs of antibodies as obtained using methods described herein. .
  • An antibody VH domain an antibody VL domain, a set of HCDRs, a set of
  • LCDRs a set of CDRs, one or more HCDRs, e.g., an HCDR3, and/or one or more LCR's, e.g., an LCDR3, may be employed in a TGF- 3 antagonist.
  • Variants of the VH and VL domains and CDRs, including those for which amino acid sequences are set out herein, and which can be employed in specific antibodies for TGF- ⁇ can be obtained by means of methods of sequence alteration or mutation and screening.
  • Variable domain amino acid sequence variants of any of the VH and VL domains whose sequences are specifically disclosed herein may be employed in the methods disclosed herein.
  • Particular variants may include one or more amino acid sequence alterations (addition, deletion, substitution and/or insertion of an amino acid residue), may be less than about 20 alterations, less than about 15 alterations, less than about 10 alterations or less than about 5, 4, 3, 2 or 1 alteration. Alterations may be made in one or more framework region and/or one or more CDR.
  • a human, humanized, chimeric or synthetic specific antibody that competes or cross-competes for binding to antigen with any specific antibody that both binds the antigen and comprises a specific antibody antigen-binding region, VH and/or VL domain disclosed herein, set of CDRs or HCDR3 disclosed herein, or a variant of any of these can be used in the methods disclosed herein.
  • Competition between antibodies may be assayed easily in vitro, for example, using ELISA and/or by tagging a specific reporter molecule to one antibody which can be detected in the presence of other untagged antibody(s), to enable identification of specific antibodies which bind the same epitope or an overlapping epitope.
  • Cross-competition between antibodies may be readily assayed by running the reverse assay, e.g., by reversing the tagged and the untagged antibodies to identify pairs that block binding in both directions.
  • An antibody comprising an antigen-binding site of an antibody that competes or cross-competes with a PET1073G12, ⁇ 1 ⁇ 74 ⁇ 9 or PET1287A10 antibody molecule, in particular PET1073G12, PET1074B9 or PET1287A10 scFv and/or IgG4 can be used for antagonizing TGF- ⁇ .
  • the antibody is a human, humanized, chimeric or synthetic antibody.
  • an antibody can be used comprising an antigen- binding site of a human, humanized, chimeric or synthetic antibody which competes or cross- competes with an antigen-binding site described herein for binding to TGF- ⁇ , wherein the antigen-binding site of the human, humanized, chimeric or synthetic antibody is composed of a VH domain and a VL domain, and wherein the VH and VL domains comprise a set of CDRs as disclosed herein.
  • One or more specific antibodies able to bind TGF- ⁇ , TGF ⁇ 2 and TGF ⁇ 3, may be obtained by a method including bringing into contact a library of antibodies and TGF- ⁇ , and selecting one or more specific antibodies of the library able to bind all of said TGF- ⁇ .
  • the library may be displayed on the surface of bacteriophage particles, each particle containing nucleic acid encoding the antibody VH variable domain displayed on its surface, and optionally also a displayed VL domain if present.
  • nucleic acid may be taken from a bacteriophage particle displaying a said selected specific antibody.
  • nucleic acid may be used in subsequent production of a specific antibody or an antibody VH variable domain (and optionally an antibody VL variable domain) by expression from a nucleic acid with the sequence of nucleic acid taken from a bacteriophage particle displaying a said selected specific antibody.
  • An antibody VH domain with the amino acid sequence of an antibody VH domain of a said selected specific antibody may be provided in isolated form, as may a specific antibody comprising such a VH domain.
  • Ability to bind all three isoforms of TGF- ⁇ may be further tested, also ability to compete or cross-compete with PET1073G12,
  • PET1074B9 or PET1287A10 (e.g., in scFv format and/or IgG format, e.g., IgG4) for binding to all three human isoforms of TGF- ⁇ .
  • An antibody for use as a TGF-/3 antagonist may bind TGF- ⁇ 1 , TGF ⁇ 2 and/or TGF-P3 with the affinity of a PET1073G12, PET1074B9 or PET1287A10 antibody molecule, e.g., scFv, or preferably IgG4, or with an affinity that is greater than one of the above molecules.
  • a useful antibody may neutralize TGF- ⁇ , TGF ⁇ 2 and/or TGF ⁇ 3 with the potency of a PET1073G12, PET1074B9 or PET1287A10 antibody molecule, e.g., scFv, or preferably PET1073G12, PET1074B9 or PET1287A10 IgG4, or with a potency that is greater than one of the above molecules.
  • a PET1073G12, PET1074B9 or PET1287A10 antibody molecule e.g., scFv, or preferably PET1073G12, PET1074B9 or PET1287A10 IgG4, or with a potency that is greater than one of the above molecules.
  • An antibody for use as a TGF-/3 antagonist may neutralize naturally-occurring TGF- ⁇ with the potency of a PET1073G12, PET1074B9 or PET1287A10 antibody molecule, e.g., scFv, or preferably IgG4, or with a potency that is greater than one of the above molecules. Binding affinity and neutralization potency of different specific antibodies can be as compared under appropriate conditions.
  • An antibody for use as a TGF-/3 antagonist includes human, humanized, chimeric or synthetic antibodies that can neutralize naturally-occurring TGF- ⁇ with a potency that is equal to or greater than the potency of a TGF- ⁇ antigen-binding site formed by PET1073G12, PET1074B9 or PET1287A10 VH domain and the corresponding
  • PET1073G12, PET1074B9 or PET1287A10 VL domain are examples of PET1073G12, PET1074B9 or PET1287A10 VL domain.
  • an antibody for use as a TGF-/3 antagonist may comprise other amino acids, e.g., forming a peptide or polypeptide, such as a folded domain, or to impart to the molecule another functional characteristic in addition to ability to bind antigen.
  • Specific antibodies may carry a detectable label, or may be conjugated to a toxin or a targeting moiety or enzyme (e.g., via a peptidyl bond or linker).
  • An antigen-binding antibody comprises an antigen-binding site.
  • An antigen- binding site may also be provided by means of arrangement of CDRs on non-antibody protein scaffolds, such as fibronectin or cytochrome B, etc.
  • non-antibody protein scaffolds such as fibronectin or cytochrome B, etc.
  • Koide et al. (1998) Journal of Molecular Biology, 284:1141-1151; Nygren et al. (1997) Current Opinion in Structural Biology, Vol. 7:463-469). Scaffolds for engineering novel binding sites in proteins have been reviewed in detail by Nygren et al., supra.
  • Protein scaffolds for antibody mimics are disclosed in WO 00/34784, which describes proteins (antibody mimics) that include a fibronectin type ⁇ domain having at least one randomised loop.
  • a suitable scaffold into which to graft one or more CDRs e.g., a set of HCDRs, may be provided by any domain member of the
  • An advantage of a non-antibody protein scaffold is that it may provide an antigen-binding site in a conserved framework region that is smaller and/or easier to manufacture than at least some antibody molecules. Small size of an antibody may confer useful physiological properties, such as an ability to enter cells, penetrate deep into tissues or reach targets within other structures, or to bind within protein cavities of the target antigen.
  • proteins include the IgG-binding domains of protein A from S. aureus, transferrin, tetranectin, fibronectin (e.g., 10th fibronectin type ⁇ domain) and lipocalins.
  • Other approaches include synthetic "Microbodies" (Selecore GmbH), which are based on cyclotides—small proteins having intra-molecular disulphide bonds.
  • an antibody may comprise other amino acids, e.g., forming a peptide or polypeptide, such as a folded domain, or to impart to the molecule another functional characteristic in addition to ability to bind antigen.
  • Antibodies may carry a detectable label, or may be conjugated to a toxin or a targeting moiety or enzyme (e.g., via a peptidyl bond or linker).
  • an antibody may comprise a catalytic site (e.g., in an enzyme domain) as well as an antigen-binding site, wherein the antigen-binding site binds to the antigen and thus targets the catalytic site to the antigen.
  • the catalytic site may inhibit biological function of the antigen, e.g., by cleavage.
  • CDRs can be carried by scaffolds, such as fibronectin or cytochrome B (Haan & Maggos, 2004 BioCentury, 12(5): A1-A6; Koide et al., supra; Nygren et al., supra), the structure for carrying a CDR or a set of CDRs will generally be of an antibody heavy or light chain sequence or substantial portion thereof in which the CDR or set of CDRs is located at a location corresponding to the CDR or set of CDRs of naturally- occurring VH and VL antibody variable domains encoded by rearranged immunoglobulin genes.
  • immunoglobulin variable domains may be determined by reference to Kabat, et al., 1987, and updates thereof, now available on the Internet (URL: immuno.bme.nwu.edu or find "Kabat” using any search engine).
  • human hybridomas can be made as described by Kontermann et al. (Kontermann R and Dubel Stefan; Antibody
  • Synthetic antibody molecules created by expression from genes generated by means of oligonucleotides synthesized and assembled within suitable expression vectors for example, as described by Knappik et al., supra or Krebs et al., Journal of Immunological Methods 254:67-84 (2001), can be used as TGF-/3 antagonists.
  • Fragments of a whole antibody can perform the function of binding antigens.
  • binding fragments are (i) the Fab fragment consisting of VL, CL, VFf and CHI domains; (ii) the Fd fragment consisting of the VH and CHI domains; (iii) the Fv fragment consisting of the VL and VH domains of a single antibody; (iv) the dAb fragment (Ward, E. S. et al., Nature 341, 544-546 (1989), McCafferty et al.
  • Fv, scFv or diabody molecules may be stabilized by the incorporation of disulphide bridges linking the VH and VL domains (Y. Reiter et al., Nature Biotech, 14, 1239-1245, 1996).
  • Minibodies comprising a scFv joined to a CH3 domain may also be made (S. Hu et al., Cancer Res., 56, 3055-3061, 1996).
  • a dAb domain antibody is a small monomelic antigen-binding fragment of an antibody, namely the variable region of an antibody heavy or light chain (Holt et al., 2003). VH dabs occur naturally in camelids (e.g., camel, llama) and may be produced by
  • An antibody may be a dAb comprising a VH or VL domain substantially as set out herein, or a VH or VL domain comprising a set of CDRs substantially as set out herein.
  • bispecific antibodies are to be used, these may be conventional bispecific antibodies, which can be manufactured in a variety of ways (Holliger, P. and Winter G. Current Opinion Biotechnol. 4, 446-449 (1993)), e.g., prepared chemically or from hybrid hybridomas, or may be any of the bispecific antibody fragments mentioned above.
  • bispecific antibodies include those of the BiTETM technology in which the binding domains of two antibodies with different specificity can be used and directly linked via short flexible peptides. This combines two antibodies on a short single polypeptide chain. Diabodies and scFv can be constructed without an Fc region, using only variable domains, potentially reducing the effects of anti-idiotypic reaction.
  • Bispecific diabodies as opposed to bispecific whole antibodies, may also be particularly useful because they can be readily constructed and expressed in E. coli.
  • Diabodies (and many other polypeptides, such as antibody fragments) of appropriate binding specificities can be readily selected using phage display (WO94/13804) from libraries. If one arm of the diabody is to be kept constant, for instance, with a specificity directed against TGF-/3, then a library can be made where the other arm is varied and an antibody of appropriate specificity selected. Bispecific whole antibodies may be made by knobs-into- holes engineering (C. E. B. Ridgeway et al., Protein Eng., 9, 616-621, 1996).
  • Antibodies may be glycosylated, either naturally or by systems of various eukaryotic cells (e.g., CHO or NSO (ECACC 85110503) cells, or they may be (for example, if produced by expression in a prokaryotic cell) unglycosylated. Glycosylation may also be intentionally altered, for example, by inhibiting fucosylation, increase ADCC activity of the resulting antibody. Accordingly, antibodies may be expressed so as to minimize or eliminate fucosylation.
  • various eukaryotic cells e.g., CHO or NSO (ECACC 85110503) cells
  • Glycosylation may also be intentionally altered, for example, by inhibiting fucosylation, increase ADCC activity of the resulting antibody. Accordingly, antibodies may be expressed so as to minimize or eliminate fucosylation.
  • the CDR or VH or VL domain will be either identical or highly similar to the specified regions of which the sequence is set out herein. It is contemplated that from 1 to 5, preferably from 1 to 4 or 1 or 2, or 3 or 4, amino acid substitutions may be made in the CDR and/or VH or VL domains. VH or VL domains and CDRs and sets of CDRs that are highly similar to those for which sequences are given herein are encompassed by aspects, as are those with sequences that are substantially as set out herein.
  • the structure for carrying a CDR or a set of CDRs will generally be of an antibody heavy or light chain sequence or substantial portion thereof in which the CDR or set of CDRs is located at a location corresponding to the CDR or set of CDRs of naturally- occurring VH and VL antibody variable domains encoded by rearranged immunoglobulin genes.
  • the structures and locations of immunoglobulin variable domains may be determined by reference to Kabat, E. A. et al., Sequences of Proteins of Immunological Interest. 4th Edition. US Department of Health and Human Services. 1987, and updates thereof, now available on the Internet (URL: immuno.bme.nwu.edu or find "Kabat" using any search engine).
  • CDRs are defined according to Kabat et al. CDRs can also be carried by other scaffolds, such as fibronectin or cytochrome B.
  • a CDR amino acid sequence substantially as set out herein is carried as a CDR in a human variable domain or a substantial portion thereof.
  • the HCDR3 sequences substantially as set out herein represent preferred embodiments and it is preferred that each of these is carried as a HCDR3 in a human heavy chain variable domain or a substantial portion thereof.
  • Variable domains employed may be obtained or derived from any germ-line or rearranged human variable domain, or may be a synthetic variable domain based on consensus or actual sequences of known human variable domains.
  • a CDR sequence e.g., CDR3
  • CDR3 may be introduced into a repertoire of variable domains lacking a CDR (e.g., CDR3), using recombinant DNA technology.
  • Preferred germline frameworks have been identified already herein.
  • the repertoire may then be displayed in a suitable host system, such as the phage display system of WO92/01047 or any of a subsequent large body of literature, including Kay, B. K., Winter, J., and McCafferty, J. (1996) Phage Display of Peptides and Proteins: A Laboratory Manual, San Diego: Academic Press, so that suitable antibodies may be selected.
  • a repertoire may consist of from 10 4 individual members upwards, for example, from 10 6 to 10 8 or 10 10 members.
  • Other suitable host systems include yeast display, bacterial display, T7 display, ribosome display, covalent display and so on.
  • a further alternative is to generate novel VH or VL regions carrying CDR- derived using random mutagenesis of one or more selected VH and/or VL genes to generate mutations within the entire variable domain.
  • a technique is described by Gram et al. Proc. Natl. Acad. Sci., USA, 89:3576-3580), who used error-prone PCR.
  • one or two amino acid substitutions are made within a set of HCDRs and/or LCDRs.
  • Another method which may be used is to direct mutagenesis to CDR regions of VH or VL genes. Such techniques are disclosed by Barbas et al., (1994, Proc. Natl. Acad.
  • PET1287A10 VH domain may be subject to mutation to provide one or more VH domain amino acid sequence variants which may be combined with one or more VL domains.
  • the VH domain may have a germline sequence, and in preferred embodiments is DP-10 or DP-88.
  • a VL domain sequence may have a germline sequence, and in preferred embodiments is DPK-22.
  • PET1073G12, PET1074B9 or PET1287A10 HCDR1, HCDR2 and HCDR3, or the PET1073G12, PET1074B9 or PET1287A10 set of HCDRs may be employed, and/or one or more of PET1073G12, PET1074B9 or
  • PET1287A10 set of LCDRs.
  • a substantial portion of an immunoglobulin variable domain will comprise at least the three CDR regions, together with their intervening framework regions.
  • the portion will also include at least about 50% of either or both of the first and fourth framework regions, the 50% being the C-terminal 50% of the first framework region and the N- terminal 50% of the fourth framework region.
  • Additional residues at the N-terminal or C- terminal end of the substantial part of the variable domain may be those not normally associated with naturally-occurring variable domain regions.
  • construction of antibodies made by recombinant DNA techniques may result in the introduction of N- or C- terminal residues encoded by linkers introduced to facilitate cloning or other manipulation steps.
  • Other manipulation steps include the introduction of linkers to join variable domains to further protein sequences including immunoglobulin heavy chains, other variable domains (for example, in the production of diabodies) or protein labels.
  • Antibodies comprising a pair of VH and VL domains are preferred, single binding domains based on either VH or VL domain sequences may also be used. It is known that single immunoglobulin domains, especially VH domains, are capable of binding target antigens in a specific manner. In the case of either of the single specific binding domains, these domains may be used to screen for complementary domains capable of forming a two- domain antibody able to bind the three isoforms of human TGF- 3.
  • phage display screening methods using the so-called hierarchical dual combinatorial approach as disclosed in WO92/01047, in which an individual colony containing either an H or L chain clone is used to infect a complete library of clones encoding the other chain (L or H) and the resulting two-chain antibody is selected in accordance with phage display techniques, such as those described in that reference.
  • S antibodies may further comprise antibody constant regions or parts thereof.
  • a VL domain may be attached at its C-terminal end to antibody light chain constant domains including human C* or C ⁇ chains, preferably C K chains.
  • an antibody based on a VH domain may be attached at its C-terminal end to all or part (e.g., a CHI domain) of an immunoglobulin heavy chain derived from any antibody isotype, e.g., IgG, IgA, IgE and IgM and any of the isotype sub-classes, particularly IgGl and IgG4.
  • IgG4 is preferred. IgG4 is preferred for some applications because it does not bind complement has reduced effector functions. Where effector function is desired, IgGl is preferred. Effector function may also be increased by manipulating the glycosylation state of the antibody, such as by decreasing the fucose content, by methods which are known in the art.
  • the heavy chain may or may not have a C-terminal lysine residue. Any synthetic or other constant region variant that has these properties and stabilizes variable regions may also be used in some embodiments.
  • Heterogeneous preparations of the antibodies or antigen-binding fragments thereof may be useful.
  • such preparations may be mixtures of antibodies with full-length heavy chains and antibodies with heavy chains lacking the C-terminal lysine, with various degrees of glycosylation, with derivatized amino acids, such as cyclization of an N- terminal glutamic acid to form a pyroglutamic acid residue and/or with deamidated forms of the heavy and or light chain.
  • compositions comprising TGF- 3 antibodies may be administered to individuals in need thereof, preferably in a "therapeutically effective amount," this being sufficient to show benefit to a patient. Such benefit may be at least amelioration of at least one symptom of a particular disease or disorder.
  • the actual amount administered, and rate and time-course of administration, will depend on the nature and severity of the disease being treated. Prescription of treatment, e.g., decisions on dosage etc, may be determined based on preclinical and clinical, studies the design of which is well within the level of skill in the art.
  • Antibodies may be administered by injection (for example, subcutaneously, intravenously, intracavity (e.g., after tumor resection), intralesionally, intraperitoneally or intramuscularly), by inhalation, or topically (for example, intraocular, intranasal, rectal, into wounds, on skin), or orally.
  • injection for example, subcutaneously, intravenously, intracavity (e.g., after tumor resection), intralesionally, intraperitoneally or intramuscularly
  • topically for example, intraocular, intranasal, rectal, into wounds, on skin
  • the precise dose will depend upon a number of factors, including, the condition and medical history of the patient, the precise nature of the antibody (e.g., whole antibody, fragment or diabody), and the nature of any detectable label or other molecule attached to the antibody.
  • a typical antibody dose will be in the range 100 ⁇ g to 1 gm for systemic applications, and 1 ⁇ g to 1 mg for topical applications.
  • the antibody will be a whole antibody, preferably the IgG4 isotype. This is a dose for a single treatment of an adult patient, which may be proportionally adjusted for children and infants, and also adjusted for other antibody formats in proportion to molecular weight and activity. Treatments may be repeated at daily, twice-weekly, weekly, monthly or other intervals, at the discretion of the physician.
  • Antibodies will usually be administered in the form of a pharmaceutical composition, which may comprise at least one component in addition to the antibody.
  • compositions for use in methods of treating AMI may comprise, in addition to active ingredient, a pharmaceutically-acceptable excipient, carrier, buffer, stabiliser or other materials well known to those skilled in the art.
  • a pharmaceutically-acceptable excipient such materials should be non-toxic and should not interfere with the efficacy of the active ingredient.
  • Such materials could include, for example, any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like that are physiologically compatible.
  • Some examples of pharmaceutically-acceptable carriers are water, saline, phosphate buffered saline, dextrose, glycerol, ethanol and the like, as well as combinations thereof.
  • isotonic agents for example, sugars, polyalcohols, such as mannitol, sorbitol, or sodium chloride in the composition.
  • additional examples of pharmaceutically-acceptable substances are wetting agents or minor amounts of auxiliary substances, such as wetting or emulsifying agents, preservatives or buffers, which enhance the shelf life or effectiveness of the antibody.
  • the precise nature of the carrier or other material will depend on the route of administration, which may be oral, topical, by inhalation or by injection, e.g., intravenous.
  • the antibody is administered by intravenous infusion or injection.
  • the antibody is administered by intramuscular or subcutaneous injection.
  • compositions for oral administration may be in tablet, capsule, powder or liquid form for example, with an inert diluent or an assimilable edible carrier.
  • a tablet may comprise a solid carrier, such as gelatin or an adjuvant.
  • Liquid pharmaceutical compositions generally comprise a liquid carrier, such as water, petroleum, animal or vegetable oils, mineral oil or synthetic oil. Physiological saline solution, dextrose or other saccharide solution or glycols, such as ethylene glycol, propylene glycol or polyethylene glycol may be included.
  • the antibody (and other ingredients, if desired) can also be enclosed in a hard or soft shell gelatin capsule, compressed into tablets, or incorporated directly into the subject's diet.
  • the active ingredient can be
  • the active ingredient will be in the form of a parenterally acceptable aqueous solution which is pyrogen- free and has suitable pK, isotonicity and stability.
  • a parenterally acceptable aqueous solution which is pyrogen- free and has suitable pK, isotonicity and stability.
  • isotonic vehicles such as Sodium Chloride Injection, Ringer's Injection, and/or Lactated Ringer's Injection.
  • Preservatives, stabilisers, buffers, antioxidants and/or other additives may be included, as required.
  • a composition may be administered alone or in combination with other treatments, either simultaneously or sequentially dependent upon the condition to be treated.
  • Antibodies may be formulated in liquid, semi-solid or solid forms, such as liquid solutions (e.g., injectable and infusible solutions), dispersions or suspensions, tablets, pills, powders, liposomes and suppositories.
  • liquid solutions e.g., injectable and infusible solutions
  • dispersions or suspensions tablets, pills, powders, liposomes and suppositories.
  • the preferred form depends on the intended mode of administration, therapeutic application, the physicochemical properties of the molecule and the route of delivery.
  • Formulations may include excipients, or combinations of excipients, for example: sugars, amino acids and surfactants.
  • Liquid formulations may include a wide range of antibody concentrations and pH. Solid formulations may be produced by, for example, lyophilization, spray drying, or drying by supercritical fluid technology.
  • compositions typically must be sterile and stable under the conditions of manufacture and storage.
  • the composition can be formulated as a solution, microemulsion, dispersion, liposome, or other ordered structure suitable to high drug concentration.
  • Sterile injectable solutions can be prepared by incorporating the antibody in the required amount in an appropriate solvent with one or a combination of ingredients enumerated above, as required, followed by filtered sterilization.
  • dispersions are prepared by incorporating the active compound into a sterile vehicle that contains a basic dispersion medium and the required other ingredients from those enumerated above.
  • the preferred methods of preparation are vacuum drying and freeze-drying that yields a powder of the active ingredient plus any additional desired ingredient from a previously sterile- filtered solution thereof.
  • the proper fluidity of a solution can be maintained, for example, by the use of a coating, such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants.
  • Prolonged absorption of injectable compositions can be brought about by including in the composition an agent that delays absorption, for example, monostearate salts and gelatin.
  • active compound of the antibody compositions may be prepared with a carrier that will protect the antibody against rapid release, such as a controlled release formulation, including implants, transdermal patches, and
  • Biodegradable, biocompatible polymers can be used, such as ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoesters, and polylactic acid. Many methods for the preparation of such formulations are patented or generally known to those skilled in the art. See, e.g., Sustained and Controlled Release Drug Delivery Systems (J. R. Robinson, ed., Marcel Dekker, Inc., New York, 1978).
  • other therapeutic regimens may be combined with the administration of an anti-TGF-/3 antibody.
  • the combined administration includes coadministration, using separate formulations or a single pharmaceutical formulation, and consecutive administration in either order, wherein preferably there is a time period while both (or all) active agents simultaneously exert their biological activities.
  • TGF- 3 antagonist For the prevention or treatment of consequences of myocardial infarction, the appropriate dosage of a TGF- 3 antagonist will depend on the condition of the patient, the severity and course of the infarction, whether the antibody is administered for preventive or therapeutic purposes, previous therapy, the patient's clinical history and response to the antibody, and the discretion of the attending physician.
  • the antagonist may be administered to the patient at one time or over a series of treatments initiating during day 0 (e.g., within about 8, 12 or 24 hours), day 1, day 2, day 3, day 4, or day 5 after an ischemic event, preferably at day 0, day 3, or day 5.
  • administration of the antagonist of TGF-/3 is commenced within about 120 hours, about 96 hours, about 72 hours, about 48 hours, within about 24 hours, about 12 hours or even within about 8 or fewer hours of onset of acute myocardial ischemia.
  • about 5 mg/kg of antibody is an initial candidate dosage for administration to the patient, whether, for example, by one or more separate administrations, or by continuous infusion post-MI.
  • a typical daily dosage might be equal to 5 mg/kg or less, depending on the factors mentioned above.
  • the treatment is sustained until a desired suppression of disease symptoms occurs.
  • the preferred dosage of the antibody will be 5 mg/kg or less administered intravenously.
  • one or more doses of about 5 mg/kg or less (or any combination thereof) may be administered to the patient.
  • other dosage regimens may be useful. The progress of this therapy is easily monitored by conventional techniques and assays.
  • Anti-TGF-/3 antibodies are useful to treat AMI when combined with antagonists of the renin-angiotensin- aldosterone system including but not limited to: renin inhibitors, angiotensin-converting enzyme (ACE) inhibitors, Ang ⁇ receptor antagonists (also known as "Ang ⁇ receptor blockers”), and aldosterone antagonists.
  • renin inhibitors angiotensin-converting enzyme (ACE) inhibitors
  • Ang ⁇ receptor antagonists also known as "Ang ⁇ receptor blockers”
  • aldosterone antagonists aldosterone antagonists.
  • Anti-TGF- ⁇ antibodies are also useful to treat AMI when combined with antagonists of the beta-adrenergic system including but not limited to the group consisting of alprenolol, bucindolol, carteolol, carvedilol, labetalol, nadolol, oxprenolol, penbutolol, pindolol, propranolol, sotalol, timolol, atenolol, betaxolol, bisoprolol, celiprolol, esmolol, metoprolol, and nebivolol.
  • antagonists of the beta-adrenergic system including but not limited to the group consisting of alprenolol, bucindolol, carteolol, carvedilol, labetalol, nadolol, oxprenolol, penbutolol, pin
  • anti-TGF- ⁇ antibodies are useful to treat AMI when combined with lipid management agents including but not limited to the group of statins consisting of lovastatin, pravastatin, simvastatin, fluvastatin, atorvastatin, cerivastatin, resuvastatin, the group of bile acid sequestrants consisting of chlestyramine, celestipol, colesevalam, the group of fibric acids consisting of gemfibrozil, fenofibrate, clofibrate, the group including nicotinic acid and niaspan, the group including the cholesterol lowering agent ezetimibe and the combination of ezetimibe and simvastatin.
  • statins consisting of lovastatin, pravastatin, simvastatin, fluvastatin, atorvastatin, cerivastatin, resuvastatin
  • the group of bile acid sequestrants consisting of chl
  • anti-TGF- ⁇ antibodies are useful to treat AMI when combined with antiplatelet agents/anticoagulants including but not limited to aspirin, the group of ADP receptor inhibitors consisting of clopidogrel, prasugrel, ticagrelor, ticlopidine, and the anticoagulant warfarin.
  • antiplatelet agents/anticoagulants including but not limited to aspirin, the group of ADP receptor inhibitors consisting of clopidogrel, prasugrel, ticagrelor, ticlopidine, and the anticoagulant warfarin.
  • Therapeutic formulations of antibodies used in treatment may be provided in a container available for intravenous treatment.
  • the formulations may also be prepared for storage by mixing an antibody having the desired degree of purity with optional
  • Acceptable carriers, excipients, or stabilizers include, but not limited to those in Remington's Pharmaceutical Sciences 16th edition, Osol, A. Ed. (1980) and in the form of lyophilized formulations or aqueous solutions.
  • Acceptable carriers, excipients, or stabilizers are nontoxic to recipients at the dosages and concentrations employed, and include buffers, such as phosphate, citrate, and other organic acids; antioxidants including ascorbic acid and methionine; preservatives (such as octadecyldimethylbenzyl ammonium chloride; hexamethonium chloride; benzalkonium chloride, benzethonium chloride; phenol, butyl or benzyl alcohol; alkyl parabens, such as methyl or propyl paraben; catechol; resorcinol;
  • low-molecular-weight polypeptides such as serum albumin, gelatin, or immunoglobulins; hydrophilic polymers, such as polyvinylpyrrolidone; amino acids, such as glycine, glutamine, asparagine, histidine, arginine, or lysine; monosaccharides, disaccharides, and other carbohydrates including glucose, mannose, or dextrins; chelating agents, such as EDTA; sugars, such as sucrose, mannitol, trehalose or sorbitol; salt-forming counter-ions, such as sodium; metal complexes; and/or non-ionic surfactants.
  • proteins such as serum albumin, gelatin, or immunoglobulins
  • hydrophilic polymers such as polyvinylpyrrolidone
  • amino acids such as glycine, glutamine, asparagine, histidine, arginine, or lysine
  • the formulation may also contain more than one active compound as necessary for the particular indication being treated.
  • the compounds with complementary activities do not adversely affect each other.
  • the composition may further comprise a cytokine, growth-inhibitory agent, anti-hormonal agent, TGF-/3 -targeted drug, anti-angiogenic agent, and/or cardioprotectant.
  • cytokine growth-inhibitory agent, anti-hormonal agent, TGF-/3 -targeted drug, anti-angiogenic agent, and/or cardioprotectant.
  • Such molecules are suitably present in combination in amounts that are effective for the purpose intended.
  • Cytokine is a generic term for proteins released by one cell population that act on another cell as intercellular mediators.
  • cytokines are lymphokines, monokines, and traditional polypeptide hormones. Included among the cytokines are growth hormone, such as human growth hormone, N-methionyl human growth hormone, and bovine growth hormone; parathyroid hormone; thyroxine; insulin; proinsulin; relaxin; prorelaxin; glycoprotein hormones, such as follicle-stimulating hormone (FSH), thyroid-stimulating hormone (TSH), and luteinizing hormone (LH); hepatic growth factor; fibroblast growth factor; prolactin; placental lactogen; tumor necrosis factor-a and - ⁇ ; mullerian-inhibiting substance; mouse gonadotropin-associated peptide; inhibin; activin; vascular endothelial growth factor; integrin; thrombopoietin (TPO); nerve growth factors,
  • growth hormone such as human
  • platelet-growth factor insulin-like growth factor-I and - ⁇ ; erythropoietin (EPO);
  • interferons such as interferon- ⁇ , ⁇ , and - ⁇ , colony-stimulating factors (CSFs), such as macrophage-CSF (M-CSF); granulocyte-macrophage-CSF (GM-CSF); and granulocyte-CSF (G-CSF); interleukins (ILs), such as IL-1, IL-la, IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, EL-8, IL-9, IL-10, IL-11, IL-12; a tumor necrosis factor, such as TNF-a or TNF-/3; and other polypeptide factors including LIF and kit ligand (KL).
  • cytokine includes proteins from natural sources or from recombinant cell culture and biologically active equivalents of the native-sequence cytokines.
  • a "cardioprotectant” is a compound or composition that prevents or reduces myocardial dysfunction (i e., cardiomyopathy and/or congestive heart failure) associated with administration of a drug, such as an anti-TGF- 3 antibody, to a patient.
  • the cardioprotectant may, for example, block or reduce a free-radical-mediated cardiotoxic effect and/or prevent or reduce oxidative-stress injury.
  • the active ingredients may also be entrapped in microcapsules prepared, for example, by coacervation techniques or by interfacial polymerization, for example, hydroxymethylcellulose or gelatin-microcapsules and poly-(methylmethacylate)
  • microcapsules respectively, in colloidal drug-delivery systems (for example, liposomes, albumin microspheres, microemulsions, nano-particles and nanocapsules) or in
  • Sustained-release preparations may be prepared. Suitable examples of sustained-release preparations may include semipermeable matrices of solid hydrophobic polymers containing the antibody, which matrices are in the form of shaped articles, e.g., films, or microcapsules. Examples of sustained-release matrices include but are not limited to, polyesters, hydrogels (for example, poly(2-hydroxyethyl-methacrylate), or
  • poly(vinylalcohol) polylactides, copolymers of L-glutamic acid and ⁇ ethyl-L-glutamate, non-degradable ethylene-vinyl acetate, degradable lactic acid-glycolic acid copolymers, and poly-D-(-)-3-hydroxybutyric acid.
  • the formulations to be used for in vivo administration must be sterile. This is readily accomplished by filtration through sterile filtration membranes.
  • An article of manufacture containing materials useful for the treatment of the MI as described above may be provided, generally comprising a container and a label or package insert on or associated with the container.
  • a "package insert” comprises instructions customarily included in commercial packages of therapeutic products, that contain
  • Suitable containers include, but are not limited to, bottles, vials, IV solution bags, vessels, syringes, etc.
  • the containers may be formed from a variety of materials, such as glass or plastic.
  • the container holds a composition that is effective for inhibition of TGF-/3 signaling and may have a sterile access port (for example, the container may be an
  • At least one active ingredient in the composition may be an anti-TGF-/3 antibody.
  • the label or package insert may indicate that the composition is used for treating myocardial infarction, acute myocardial infarction, or the reduction of a consequence of myocardial infarction, In one embodiment, the label or package insert indicates that the composition comprising the antibody can be administered during the acute phase of a myocardial infarction.
  • the article of manufacture may comprise a container comprising a composition of an anti-TGF-/3 antibody, and a therapeutic agent other than the antibody.
  • the article of manufacture may further comprise a package insert indicating that the first and second compositions can be used in combination to treat a myocardial infarction.
  • This therapeutic agent may be any of the adjunct therapies described in the preceding section (e.g., an anti-angiogenic agent, an anti-hormonal compound, a cardioprotectant, and/or a regulator of immune function in a mammal, including a cytokine).
  • the article of manufacture may further comprise a second (or third) container comprising a pharmaceutically- acceptable buffer, such as bacteriostatic water for injection (BWFI), phosphate-buffered saline, Ringer's solution and dextrose solution. It may further include other materials desirable from a commercial and user standpoint, including other buffers, diluents, filters, needles, and syringes.
  • a pharmaceutically- acceptable buffer such as bacteriostatic water for injection (BWFI), phosphate-buffered saline, Ringer's solution and dextrose solution.
  • anti-TGF-/3 antibodies can be provided in a kit, i.e., a packaged combination of reagents in predetermined amounts with instructions.
  • other additives may be included, such as stabilizers, buffers (e.g., a block buffer or lysis buffer).
  • the antibodies may be provided as dry powders, usually
  • lyophilized including excipients that on dissolution will provide a solution having the appropriate concentration.
  • a method of treating a patient suffering from myocardial infarction, acute myocardial infarction or of reducing adverse consequences of an acute myocardial infarction in a patient may comprise
  • the TGF-0 antagonist may be selected from a group consisting of: an antibody or protein comprising an antibody fragment directed against one or more iso forms of TGF- 3; a TGF- 3 receptor; an antibody or protein comprising an antibody fragment directed against one or more TGF-/3 receptors; latency associated peptide; large latent TGF-/3, a TGF-/3 inhibiting proteoglycan; somatostatin; mannose-6-phosphate; mannose-1 -phosphate; prolactin; insulinlike growth factor ⁇ ; IP- 10; an arg-gly-asp containing peptide; a plant, fungal, or bacterial extract; an antisense or interfering RNA oligonucleotide; and a protein involved in TGF-/3 signaling.
  • the antagonist of TGF- ⁇ is a humanized anti-TGF-/3 antibody or a fragment or antigen-binding site of an anti-TGF-0 antibody.
  • the TGF-/3 antagonist may be an antibody or antibody fragment capable of binding and neutralizing more than one isoform of TGF- 3.
  • the antibody may be a chimeric monoclonal antibody comprising a TGF-/3 binding portion and a remainder portion, said TGF-/3 binding portion comprising the antigen-binding portion of monoclonal antibody ID 11.16, and the remainder portion derived from one or more human antibodies.
  • An antibody that is directed against more than one isoform of TGF-/3 may be a human or humanized form of monoclonal antibody 1D1 1.16,
  • the antagonist of TGF-/3 may be an antibody or antibody fragment that neutralizes human TGF-jSl, TGF-/32 and TGF-/33
  • the administration of the antagonist of TGF-/3 may be commenced within about 120, about 80, about 72, about 48, or about 24 hours of onset of acute myocardial ischemia. In some instances, administration of the antagonist of TGF-/3 is commenced within about 12 hours of onset of acute myocardial ischemia. Administration of the antagonist of TGF-/3 may be commenced prior to substantial macrophage and mononuclear infiltration of tissue affected by the myocardial infarction. In other instances, administration of the antagonist of TGF-0 is commenced during a period characterized by neutrophilic infiltration of tissue affected by the myocardial infarction. Further, in some instances administration of the antagonist of TGF-/3 is commenced during a period characterized by necrosis of tissue affected by the myocardial infarction.
  • the method can also comprise administering a compound capable of selectively restoring a desirable function of TGF-/5 to a patient diagnosed with an acute myocardial infarction during the acute stage of the myocardial infarction, for example, an anti-inflammatory drug and/or an antagonist of TNF- ⁇ .
  • a compound capable of selectively restoring a desirable function of TGF-/5 to a patient diagnosed with an acute myocardial infarction during the acute stage of the myocardial infarction, for example, an anti-inflammatory drug and/or an antagonist of TNF- ⁇ .
  • the method may be used in human and veterinary medicine so that the patient may be a human or a non-human mammal.
  • the antagonist is an antibody that neutralizes human TGF-/31, TGF-/32 and TGF-/33, and comprises an antigen-binding domain of an antibody, wherein said antigen-binding domain comprises a set of CDRs HCDR1, HCDR2 and HCDR3, and wherein said antigen-binding domain utilizes a human VHl family gene and wherein said HCDR3 has an amino acid sequence selected from the group consisting of SEQ ID NO: 5, SEQ ID NO: 15 and SEQ ID NO: 25.
  • the human VHl family gene can be a human VHl -2 gene, which in some instances may be a DP- 10 or a DP-88 gene.
  • the antigen-binding domain may further comprise a set of CDRs LCDR1, LCDR2 and LCDR3, and wherein said antigen-binding domain utilizes a human VK3 family gene and wherein said LCDR3 has an amino acid sequence selected from the group consisting of SEQ ID NO: 10, SEQ ID NO: 20 and SEQ ID NO: 30.
  • the HCDR3 and LCDR3 can be selected from the group consisting of: (a) SEQ ID NO: 5 and SEQ ID NO: 10, respectively; (b) SEQ ID NO: 15 and SEQ ID NO: 20, respectively; and (c) SEQ ID NO: 25 and SEQ ID NO: 30, respectively.
  • the human VK3 family gene may be a human VK
  • the HCDR1, HCDR2 and HCDR3 of the VH domain may be comprised within a germline heavy chain framework, or the HCDR1, HCDR2 and HCDR3 of the VH domain are within a framework that comprises up to 12 mutations from the germline amino acid sequence.
  • the LCDRl, LCDR2 and LCDR3 of the V/c domain may be comprised within a germline heavy chain framework. In some instances, the LCDRl, LCDR2 and LCDR3 of the V/c domain may be within a framework that comprises up to 5 mutations from the germline VK amino acid sequence.
  • the antagonist of TGF-/3 may be an antibody that neutralizes human TGF-/31, TGF-/32 and TGF-/33, and comprises an antigen-binding domain of an antibody, wherein said antigen-binding domain utilizes a human VH DP-10 gene or a human VH DP-88 gene and comprises an FR4 amino acid sequence comprising the amino acid sequence in SEQ ID NO: 31,
  • the antigen-binding domain may utilize a human VH DP-10 gene or a human VH DP-88 gene, and comprises a set of CDRs HCDR1, HCDR2 and HCDR3, wherein said HCDR3 has an amino acid sequence selected from the group consisting of SEQ ID NO: 5, SEQ ID NO: 15 and SEQ ID NO: 25, and further comprises an FR4 amino acid sequence comprising the amino acid sequence in SEQ ID NO: 31.
  • the antigen-binding domain may further utilize a human V/c 3 family gene and a human J/c5 gene.
  • An antigen-binding domain utilizing a human V/c3 family gene and a human J/c5 gene may comprise a set of CDRs LCDRl, LCDR2 and LCDR3, wherein said LCDR3 has an amino acid sequence selected from the group consisting of SEQ ID NO: 10, SEQ ID NO: 20 and SEQ ID NO: 30.
  • the antagonist of TGF-3 neutralizes human TGF-/31, TGF-/32 and TGF-/53, and comprises an antigen-binding domain of an antibody, wherein said antigen-binding domain comprises: (a) the HCDRl of amino acid sequence of SEQ ID NO: 3, HCDR2 of amino acid sequence of SEQ ID NO: 4, HCDR3 of amino acid sequence of SEQ ID NO: 5; (b) the HCDRl of amino acid sequence of SEQ ID NO: 13, HCDR2 of amino acid sequence of SEQ ID NO: 14, HCDR3 of amino acid sequence of SEQ ID NO: 15; or (c) the HCDRl of amino acid sequence of SEQ ED NO: 23, HCDR2 of amino acid sequence of SEQ ID NO: 24, HCDR3 of amino acid sequence of SEQ ID NO: 25.
  • the antigen-binding domain may further comprise an antibody VL domain.
  • the antigen-binding domain may comprise LCDRs selected from the group consisting of: (a) the LCDR1 of amino acid sequence of SEQ ID NO: 8, LCDR2 of amino acid sequence of SEQ ID NO: 9, LCDR3 of amino acid sequence of SEQ ID NO: 10; (b) the LCDR1 of amino acid sequence of SEQ ID NO: 18, LCDR2 of amino acid sequence of SEQ ID NO: 19, LCDR3 of amino acid sequence of SEQ ID NO: 20; and (c) the LCDR1 of amino acid sequence of SEQ ID NO: 28, LCDR2 of amino acid sequence of SEQ ID NO: 29, LCDR3 of amino acid sequence of SEQ ID NO: 30.
  • the HCDRl, HCDR2 and HCDR3 of the VH domain may be comprised within a germline heavy chain framework, for example, a human VH1 family framework.
  • HCDRl, HCDR2 and HCDR3 of the VH domain may be within germline human heavy chain framework VH1 DP- 10 or DP-88.
  • the LCDR1, LCDR2 and LCDR3 of the VL domain may be within a germline light chain framework.
  • the germline light chain framework may be a human VK3 family framework.
  • the antigen-binding domain may further comprise a human JK5 gene.
  • the human VK3 family gene may be a VK DPK22 gene.
  • the antagonist of TGF-/3 may be an antibody comprising the PET1073G12 VH domain (SEQ ID NO: 2) with up to 5 mutations, or an antigen-binding portion thereof.
  • the antagonist of TGF-0 may be an antibody comprising the PET1074B9 VH domain (SEQ ED NO: 12) with up to 5 mutations, or an antigen-binding portion thereof.
  • the antagonist of TGF-/3 may be an antibody comprising the PET1287A10 VH domain (SEQ ID NO: 22) with up to 5 mutations, or an antigen-binding portion thereof.
  • the antagonist of TGF- 3 may be an antibody comprising the PET1073G12 VL domain (SEQ ID NO: 7) with up to 5 mutations, or an antigen-binding portion thereof.
  • the antagonist of TGF-/3 may be an antibody comprising the PET1074B9 VL domain (SEQ ID NO: 17) with up to 5 mutations ⁇ or an antigen-binding portion thereof.
  • the antagonist of TGF-/3 may be an antibody comprising the PET1287A10 VL domain (SEQ ID NO: 27) with up to 5 mutations, or an antigen-binding portion thereof.
  • the antagonist of TGF-/3 may be an antibody comprising the PET 1073G12 VH domain (SEQ ED NO: 2) and the PET 1073G12 VL domain (SEQ ED NO: 7).
  • the antagonist of TGF-/3 may be an antibody comprising the PET 1074B9 VH domain (SEQ ED NO: 12) and the PET 1074B9 VL domain (SEQ ED NO: 17).
  • the antagonist of TGF-jS may be an antibody comprising the PET 1287A10 VH domain (SEQ ED NO: 22) and the PET 1287A10 VL domain (SEQ ED NO: 27). Further variations as described herein are also contemplated.
  • SEQ ED NOs refer to the sequences found in the attached sequence listing, which forms part of this disclosure. While the methods have been described in detail with reference to certain embodiments thereof, it will be apparent to one skilled in the art that various changes can be made, and equivalents employed, without departing from the scope of this disclosure or the claims which follow. Moreover, the following examples are presented as illustrations of aspects of the methods and should not be construed as limiting.
  • Monoclonal antibodies 1D11 and GC 1008 were purified either from culture supernatant or ascites by protein A-Sepharose chromatography (Goding, J Immunol Meth (1976) 42; 17) (Pharmacia Fien Chemicals, Uppsala, Sweden). The binding of the gamma ( ⁇ )1 subclass and gamma ( ⁇ )4 subclass monoclonal antibodies, 1D11 and GC 1008, to protein A were enhanced by addition of a commercially prepared binding buffer (BioRad, Richmond, Calif).
  • Antibodies were eluted from the protein A-Sepharose with 0.05 M glycine-HCl plus 0.15 M NaCl buffer (pH 2.3), dialyzed overnight versus PBS and NaCl buffer (pH 2.3), dialyzed overnight versus PBS and stored at -20 degrees Celsius.
  • the gamma ( ⁇ ) 1 and gamma (7) 4 subclass antibodies purified from supernatants were concentrated and partially purified by ammonium sulfate precipitation (50% saturated) prior to protein A- chromatography.
  • EXAMPLE 2 Effect of a TGF-jS inhibitor in a rat model of cardiac ischemia reperfusion
  • AAR area at risk
  • DO left descending coronary artery
  • the microspheres distributed homogenously in the blood and lodged in capillaries of the heart and other organs and tissues.
  • the AAR in the heart was defined as the area of the myocardial tissue that did not receive any microspheres (or blood) during the ligation period.
  • the animal was lightly anesthetized with isoflurane and the heart rate was maintained at 350+50 bpm.
  • An echocardiograph was then performed in the long axis view in order to assess regional and global cardiac function. Following the echocardiography examination, the animal was euthanized with an overdose of sodium pentobarbital. The heart was then excised for histological analysis.
  • Cardiac function parameters were assessed by echocardiography at 4 weeks following I/R, as seen in Table 1. Ejection fraction and fractional shortening represent global cardiac function. AWT, PWT and AWT/PWT (regional wall motion score) represent regional cardiac function. In the normal rodent, AWT is approximately equal to, and can be greater than, PWT. It follows then that the ratio of AWT/PWT, what we have termed regional wall motion score, in a normal animal would be ⁇ . In Table 1 , the normal animal group showed AWT greater than PWT, and regional wall motion score (AWT/PWT) of 1.7 ⁇ 0.2.
  • AWT is markedly less than PWT in the negative-control 13C4 and vehicle groups (Table 1 and Figure 2) and regional wall motion scores were 0.7 ⁇ 0.1 and 0.51 ⁇ 0.2 in the 13C4 and vehicle groups, respectively, compatible with significant impairment as compared to the ID 11 -treated groups and normal animals.
  • the relative lack of impairment in regional cardiac function in the 1D11 -treated groups was consistent with the reductions in fibrosis observed in these groups as compared to the vehicle and negative-control antibody 13C4 groups.
  • IDl 1-D3 and IDl 1-D5 groups While the level of fibrosis in IDl 1-D3 and IDl 1-D5 groups were similar, the IDl 1-D5 group reached statistical significance as compared to the negative-control 13C4 group (p ⁇ 0.05). It has been shown in MI models that the development of fibrosis post-MI is associated with upregulation of TGF- ⁇ , TGF-/3 signaling through the smad pathway and TGF- 3 regulated genes.
  • Administration of IDl 1 in rodent cardiac I/R model blunts the upregulation of TGF-/3 and TGF-/3 associated genes following I/R, including collagen 3 and fibronectin which are associated with fibrosis. The observed reduction in fibrosis with IDl 1 administration is consistent with IDl 1 blunting of TGF- ⁇ mediated fibrosis in this model.
  • ID 11 -mediated TGF-/3 antagonism beginning at either day 3 or day 5 post I/R resulted in reductions in cardiac fibrosis which reached significance in the 1D11-D5 group.
  • the reductions in fibrosis corresponded with improved regional cardiac function as compared to animals that received the negative-control antibody, 13C4, or vehicle, and suggested sparing or salvage of myocardium in the 1D11 -treated animals.
  • EXAMPLE 3 Effect of timing of administration of a TGF-/3 inhibitor in a rat model of cardiac ischemia reperfusion
  • negative-control antibody 13C4 or vehicle was administered by intravenous (IV) injection, and then readministered every 3rd day until day 28,
  • microspheres were labeled with a yellow fluorochrome and were then injected into the LV of the heart. This was done immediately before releasing the temporary ligation of the left descending coronary artery. The microspheres distributed homogenously in the blood and lodged in capillaries of the heart, and other organs and tissues.
  • the AAR in the heart was defined as the area of the myocardial tissue that did not receive any microspheres (or blood) during the ligation period.
  • the animal was lightly anesthetized with isoflurane and the heart rate was maintained at 350 ⁇ 50 bpm. Echocardiography was then performed in the long axis view for regional and global cardiac function. Following the echocardiography examination, the animal was euthanized with an overdose of sodium pentobarbital. The heart was then excised, weighed and then processed for histological analysis. The AAR was assigned a qualitative score. Animals with small AAR ( ⁇ 20% of the LV) or no AAR were removed from study analysis
  • Cardiac fibrosis in the LV was assessed histologically and using heart weight and expressed as a percentage of fibrosis weight/total LV weight.
  • Regional cardiac function was assessed by evaluation of the anterior wall thickening (AWT) as compared to posterior wall thickening (PWT) in the area at risk. Wall thickening is the difference in the wall thickness at systole and the wall thickness at diastole.
  • AAT anterior wall thickening
  • PWT posterior wall thickening
  • Wall thickening is the difference in the wall thickness at systole and the wall thickness at diastole.
  • Global function was assessed by evaluation of ejection fraction (EF) and fractional shortening (FS).
  • the 1D11-D5 group also showed significant improvements in the global cardiac function parameters of ejection fraction and fractional shortening as compared to the vehicle control (Table 2), which is consistent with the fibrosis and regional cardiac function assessments.
  • the other 1D11-treated groups did not demonstrate changes in global function as compared to the vehicle and matched 13C4 groups.
  • Reduction in fibrosis with relative lack of impairment in regional function in ID 11-treated animals without significant improvements in global cardiac function was also observed in a previous study and is likely . attributable to compensation in function of the LV that was not infarcted in the matched 13C4 and vehicle groups making it difficult to detect changes between the groups at this time point.
  • the increase in PWT, compatible with hypertrophy, observed in these groups is consistent with this interpretation.
  • This example compared the bioactivity of the anti-TGF- ⁇ antibody, 1D11, starting at different time points post-myocardial infarction in a rat model of myocardial infarction where animals underwent cardiac ischemia followed by reperfusion. It is possible that TGF-/3 plays different roles in the repair response at DO, Dl and at D5, and that TGF-/3 antagonism initiating at these different time points results in a differential response.
  • the 1D11-Dl group showed trends towards reduction in fibrosis and improvement in cardiac function.
  • the reductions in fibrosis corresponded with significantly improved regional cardiac function as compared to animals that received the negative-control antibody, 13C4, or vehicle, as well as significantly improved global cardiac function as compared to the vehicle control in the 1D1 1-D5 group.
  • EXAMPLE 4 Effects of TGF-B Inhibitor, 1D11, in a rodent model of myocardial remodeling following myocardial ischemia
  • a dobutamine stress test was also performed. After completing all of the above procedures, the rats were euthanized, and myocardial tissues from ischemic and non-ischemic zones were collected for pathological analysis. A subgroup of nine rats was used for the assessment of infarct size was and euthanized at seven days after CAO/CAR. The hearts were then perfused and stained. The area at risk andinfarct size were measured and compared between the vehicle and IDl 1 (25 mg/kg) groups.
  • LVEF Left ventricular ejection fraction
  • IVRT isovolumic relaxation time
  • TGF-/3 antagonism utilizing 1D11 at the 5 mg/kg dose, was effective in preventing the adverse effects of remodeling following myocardial infarction in the rat.
  • the significant reductions of LV scar volume and apoptosis were consistent with the improvements in cardiac systolic and diastolic function in this model.
  • the high dose of the drug elicited opposite, adverse effects on histological and functional endpoints.
  • EXAMPLE 5 Effects of TGF-B Inhibitor, 1D11, on myocardial preservation in a rodent model of myocardial ischemia followed by reperfusion
  • microspheres that were labeled with a yellow fluorochrome were injected into the LV of the heart. This was done immediately before releasing the temporary ligation of the left descending coronary artery. The microspheres distributed homogenously in the blood and lodged in capillaries of the heart, and other organs and tissues. The AAR in the heart was defined as the area of the myocardial tissue that did not receive any microspheres (or blood) during the ligation period.
  • the animal was lightly anesthetized with isoflurane and the heart rate was maintained at 350+50 bpm. Echocardiography was then performed in the long axis view for regional cardiac function. Following the echocardiography examination, the animal was euthanized with an overdose of sodium pentobarbital. The heart was then excised, weighed and then processed for histological analysis. The AAR was assessed
  • Cardiac fibrosis in the LV was assessed histologically and using heart weight and expressed as a percentage of fibrosis weight/total LV weight.
  • Regional cardiac function was assessed by evaluation of the anterior wall thickening (AWT) as compared to posterior wall thickening (PWT) in the area at risk.
  • AKT anterior wall thickening
  • PWT posterior wall thickening
  • Wall thickening is the difference in the wall thickness at systole and the wall thickness at diastole.
  • cardiac function expressed as regional wall motion score showed less impairment in all ID 11 -treated groups (1 and 5 mg/kg doses from both formulations) as compared to the 13C4 and vehicle controls ( Figure 17).
  • This example evaluated the bioactivity of the TGF- ⁇ antagonist antibody, 1D11, at two doses (1 and 5 mg/kg) and from two different formulations, initiated 5 days following myocardial ischemia followed by reperiusion. Both the 1 and 5 mg/kg 1D11 doses from both formulations significantly reduced fibrosis and more importantly, preserved myocardium in the AAR as compared to the negative controls. Consistent with these improvements, regional cardiac function was also improved as compared to the negative controls.
  • Example 6 Effects of TGF-B inhibitor, 1D11, on cardiac expression of TGF-B and related genes in a rodent model of myocardial ischemia followed by reperfusion
  • 1D11 a TGF- ⁇ inhibitor, reduced cardiac expression of TGF- ⁇ and related genes, consistent with its effects on myocardial remodeling, myocardial preservation and myocardial function as observed in the previous examples.
  • I/R reperfusion
  • two different doses (5 or 50 mg/kg) of 1D11 were administrated via IV and continued every 3 days until either day 7 or day 12 for animals that received 5 mg/kg 1D11, or until day 12 for animals that received 50 mg/kg 1D11. Another group of animals that underwent I/R did not receive any treatment.
  • RT-PCR reverse transcriptase-polymerase chain reaction
  • the serum IDl 1 level in animals that received the 50 mg/kg IDl 1 dose and was euthanized on day 12 was approximately 1.5 times that of the animals that received 5 mg/kg 1D11 and were euthanized on the same day.
  • the lack of proportionality in the 1D11 serum levels as compared to dose may be attributable to faster clearance of 1D11 in animals that received the high dose (50 mg/kg) of 1D11.
  • Osteopontin is a potential serum marker of ID 11 -mediated modulation of fibrosis in cardiac I/R. Serum osteopontin levels were similar in normal animals, I/R animals that did not receive any treatment and were euthanized on day 12, and I/R animals that received two 5 mg/kg doses of 1D11 and were euthanized on day 7 (Figure 19). There were trends towards decreases in osteopontin levels in I/R animals that received either three 5 mg/kg 1D11 doses and were euthanized on day 12, or three 50 mg/kg doses of ID 11 and were euthanized on day 12.
  • TGF- ⁇ and related genes were analyzed by RT-PCR in the apical portion of the left ventricle, which included the area at risk and the basal portion of the LV that was not subject to ischemia. In the basal portion of the LV the expression levels of all the genes evaluated were similar to that observed in normal animals. The remainder of the descriptions of cardiac gene expression focuses on changes observed in the apical portion of the ventricle.
  • TGF- ⁇ 1 , TGF-p2 and TGF-p3 were elevated in I/R animals that did not receive any treatment and were euthanized on day 12.
  • TGF- ⁇ Compared to normal animals expression of TGF- ⁇ , TGF- 2 and TGF- 3 were increased approximately 2.3-fold, 5-fold, and 6-fold, respectively ( Figures 20-22).
  • Administration of 1D11 at 5 mg/kg reduced expression of TGF- ⁇ ⁇ , TGF-p2 and TGF-P3 ( Figures 20-22).
  • Collagen is a prominent component of fibrosis and its expression is known to be regulated by TGF- ⁇ . Cardiac expression of collagen 3 was elevated approximately 14-fold in I/R animals that did not receive any treatment compared to normal animals.
  • Endothelin-1 (ET-1) is potent vasoconstrictor whose expression is regulated by TGF- ⁇ . Cardiac expression of ET-1 was increased approximately 5.5-fold in I/R animals that did not receive any treatment compared to normal animals. Administration of 5 mg/kg IDl 1 reduced the expression of ET-1 where animals that received 3 doses of ID 11 had greater reduction in ET-1 expression compared to animals that received 2 doses of ID 11 ( Figure 24). Three 5 mg/kg IDl 1 doses nearly normalized ET-1 expression. Animals that received 50 mg/kg IDl 1 also demonstrated a reduction in ET-1 expression that was comparable to that observed in animals that received two 5 mg/kg IDl 1 doses. IDl 1-mediated inhibition of ET- 1 expression following I/R may contribute to improved perfusion in the injured myocardium and contribute to the myocardial preservation and reduced remodeling following I/R.
  • Plasminogen activator inhibitor- 1 (PAI-1) is the major inhibitor of tissue- type plasminogen activator and is regulated by TGF- ⁇ . Elevated levels of PAI-1 has been associated with increased atherothrombotic events and vascular disease. Cardiac expression of PAI-1 was increased approximately 6-fold in VR animals that did not receive any treatment as compared to normal animals. Administration of 5 mg/kg IDl 1 reduced the expression of PAI-1 where animals that received 3 doses of ID 11 had much greater reduction in PAI-1 expression as compared to animals that received 2 doses of IDl 1 ( Figure 25). Animals that received 50 mg/kg IDl 1 showed marginal reduction in PAI-1 expression.
  • IDl 1 -mediated reduction in PAI-1 expression following I/R contributed to the improvements in remodeling and myocardial preservation.
  • the 50 mg/kg IDl 1 dose appeared to have a much less robust effect on reducing PAI-1 expression compared to the 5 mg/kg dose.
  • IDl 1 Three 5 mg/kg doses of IDl 1 apparently normalized Snail2 expression. Animals that received 50 mg/kg IDl 1 also demonstrated reductions in Snaill and Snail2 expression that were comparable to that observed in animals that received two 5 mg/kg IDl 1 doses. Increased expression of Snaill and Snail2 following I/R strongly suggest that endothelial-mesenchymal transition is contributing to cardiac fibrosis in the repair response to I/R. The ID 11 -mediated reductions in Snaill and Snail2 expression following I/R are likely a contributing mechanism to the observed reduction in cardiac fibrosis and improvement in remodeling. Interestingly, the 50 mg/kg IDl 1 dose appeared to have a less robust effect on reducing Snaill and Snail2 expression as compared to the 5 mg/kg dose.
  • a marker of mesenchymal cells that is observed in endothelial-mesenchymal transition a-smooth muscle actin ( -SMA). Cardiac expression oc-SMA was elevated approximately 4-fold in I/R animals that did not receive any treatment as compared to normal animals. Administration of 5 mg/kg IDl 1 reduced the expression of a-SMA where animals that received 3 doses of ID 11 had much greater reduction a-SMA expression as compared to animals that received 2 doses of IDl 1 ( Figure 28). Animals that received 50 mg/kg IDl 1 also demonstrated reduction in a-SMA expression that was comparable to that observed in animals that received two 5 mg/kg IDl 1 doses.
  • -SMA smooth muscle actin
  • IDl 1 reduced expression of a-SMA.
  • the 50 mg/kg IDl 1 dose appeared to have a less robust effect on reducing a-SMA expression as compared to the 5 mg/kg dose.
  • Fibronectin is considered to be a marker of epithelial-mesenchymal transition and likely is a marker endothelial-mesenchymal transition. Cardiac expression fibronectin was increased approximately 16-fold in I/R animals that did not receive any treatment as compared to normal animals. Administration of 5 mg/kg IDl 1 reduced the expression of fibronectin where animals that received 3 doses of IDl 1 had much greater reduction fibronectin expression as compared to animals that received 2 doses of IDl 1 (Figure 29). Animals that received 50 mg/kg IDl 1 also demonstrated reduction in fibronectin expression that was comparable to that observed in animals that received two 5 mg/kg IDl 1 doses.
  • the ID 11-mediated reduction in fibronectin was compatible with the IDl 1 medicated reductions in endothelial-mesenchymal transition markers Snaill, Snail2 and a-SMA.
  • the 50 mg/kg IDl 1 dose appeared to have a less robust effect on reducing fibronectin expression as compared to the 5 mg/kg dose.
  • Apoptosis contributes to loss of cardiac myocytes during cardiac remodeling. Bax is a well recognized pro-apoptotic gene and cardiac expression Bax was increased approximately 1.8-fold in I/R animals that did not receive any treatment as compared to normal animals.
  • TGF- ⁇ antagonist e.g., an anti-TGF- ⁇ antibody
  • Serum level of osteopontin may be a marker of 1D11 -mediated reduction of cardiac fibrosis.
  • TGF- ⁇ and related genes are induced in I/R and are drivers of the cardiac fibrosis and remodeling that occurs following I/R.

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